http://identifiers.org/exac.variant/10-103345845-CAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345845
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345843
    reference: chr 10
allele count: 1
allele frequency: 8.307303781484682e-6
allele num: 120376
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.182_183delTT
  hgvsp: ENSP00000359181.3:p.Phe61Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1156_66+1157delTT
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.215_216delTT
  hgvsp: ENSP00000411678.1:p.Phe72Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.182_183delTT
  hgvsp: ENSP00000359188.1:p.Phe61Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1156_60+1157delTT
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-83_-82delTT
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1186_-176-1185delAA
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.182_183delTT
  hgvsp: ENSP00000299206.4:p.Phe61Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-83_-82delTT
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.92_93delTT
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.182_183delTT
  hgvsp: ENSP00000400517.1:p.Phe61Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1156_60+1157delTT
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-83_-82delTT
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.182_183delTT
  hgvsp: ENSP00000400676.1:p.Phe61Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.182_183delTT
  hgvsp: ENSP00000414293.1:p.Phe61Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1156_60+1157delTT
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.106_107delTT
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1186_440-1185delAA
  variant of: http://identifiers.org/hgnc/24542
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe61Ter
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: CAA
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

10-103345847-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345847
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345847
    reference: chr 10
allele count: 1
allele frequency: 8.312413758707254e-6
allele num: 120302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-83T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.182T>C
  hgvsp: ENSP00000299206.4:p.Phe61Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.182T>C
  hgvsp: ENSP00000400676.1:p.Phe61Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.215T>C
  hgvsp: ENSP00000411678.1:p.Phe72Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1156T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.106T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.182T>C
  hgvsp: ENSP00000359181.3:p.Phe61Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.182T>C
  hgvsp: ENSP00000400517.1:p.Phe61Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1186A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1156T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1186A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.182T>C
  hgvsp: ENSP00000414293.1:p.Phe61Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.182T>C
  hgvsp: ENSP00000359188.1:p.Phe61Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-83T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1156T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.92T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1156T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-83T>C
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14018
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe61Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum

http://identifiers.org/exac.variant/10-103345857-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345857
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345857
    reference: chr 10
allele count: 5
allele frequency: 4.17076792178976e-5
allele num: 119882
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1146G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1176C>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.96G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1176C>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-93G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.172G>T
  hgvsp: ENSP00000359181.3:p.Ala58Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.205G>T
  hgvsp: ENSP00000411678.1:p.Ala69Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1146G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-93G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.172G>T
  hgvsp: ENSP00000359188.1:p.Ala58Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.172G>T
  hgvsp: ENSP00000400517.1:p.Ala58Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1146G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.172G>T
  hgvsp: ENSP00000414293.1:p.Ala58Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.172G>T
  hgvsp: ENSP00000299206.4:p.Ala58Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.82G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.172G>T
  hgvsp: ENSP00000400676.1:p.Ala58Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1146G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-93G>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala58Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-103345859-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345859
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345859
    reference: chr 10
allele count: 4
allele frequency: 3.33889816360601e-5
allele num: 119800
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.170G>A
  hgvsp: ENSP00000359188.1:p.Arg57Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1144G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.94G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.170G>A
  hgvsp: ENSP00000400517.1:p.Arg57Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1174C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-95G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.170G>A
  hgvsp: ENSP00000359181.3:p.Arg57Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-95G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.170G>A
  hgvsp: ENSP00000299206.4:p.Arg57Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.203G>A
  hgvsp: ENSP00000411678.1:p.Arg68Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.80G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.170G>A
  hgvsp: ENSP00000414293.1:p.Arg57Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.170G>A
  hgvsp: ENSP00000400676.1:p.Arg57Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1144G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1144G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1144G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1174C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-95G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg57Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

10-103345860-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345860
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345860
    reference: chr 10
allele count: 140
allele frequency: 1.168809484054099e-3
allele num: 119780
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.93C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1143C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.169C>T
  hgvsp: ENSP00000359181.3:p.Arg57Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.202C>T
  hgvsp: ENSP00000411678.1:p.Arg68Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1173G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1143C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.169C>T
  hgvsp: ENSP00000414293.1:p.Arg57Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1143C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-96C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.169C>T
  hgvsp: ENSP00000359188.1:p.Arg57Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.169C>T
  hgvsp: ENSP00000400517.1:p.Arg57Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-96C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.79C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1173G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1143C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.169C>T
  hgvsp: ENSP00000299206.4:p.Arg57Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.169C>T
  hgvsp: ENSP00000400676.1:p.Arg57Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-96C>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
hgvs: p.Arg57Trp
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD

10-103345866-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345866
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345866
    reference: chr 10
allele count: 4
allele frequency: 3.345264777707156e-5
allele num: 119572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-102C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-102C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.163C>T
  hgvsp: ENSP00000299206.4:p.Arg55Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.163C>T
  hgvsp: ENSP00000359188.1:p.Arg55Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.196C>T
  hgvsp: ENSP00000411678.1:p.Arg66Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.163C>T
  hgvsp: ENSP00000359181.3:p.Arg55Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.87C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.163C>T
  hgvsp: ENSP00000400676.1:p.Arg55Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1167G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.163C>T
  hgvsp: ENSP00000414293.1:p.Arg55Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1137C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-102C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1137C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1137C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.73C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1137C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1167G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.163C>T
  hgvsp: ENSP00000400517.1:p.Arg55Ter
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg55Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

10-103345877-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345877
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345877
    reference: chr 10
allele count: 5
allele frequency: 4.198011821601289e-5
allele num: 119104
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-113C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1126C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.62C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-113C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.152C>T
  hgvsp: ENSP00000400676.1:p.Thr51Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.185C>T
  hgvsp: ENSP00000411678.1:p.Thr62Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-113C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.76C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.152C>T
  hgvsp: ENSP00000359188.1:p.Thr51Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.152C>T
  hgvsp: ENSP00000400517.1:p.Thr51Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.152C>T
  hgvsp: ENSP00000299206.4:p.Thr51Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1156G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1126C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.152C>T
  hgvsp: ENSP00000414293.1:p.Thr51Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.152C>T
  hgvsp: ENSP00000359181.3:p.Thr51Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1126C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1156G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1126C>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr51Ile
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS

10-103345880-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345880
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345880
    reference: chr 10
allele count: 5
allele frequency: 4.205073000067281e-5
allele num: 118904
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.73G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-116G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1123G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.182G>A
  hgvsp: ENSP00000411678.1:p.Arg61His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.149G>A
  hgvsp: ENSP00000299206.4:p.Arg50His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.149G>A
  hgvsp: ENSP00000414293.1:p.Arg50His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.149G>A
  hgvsp: ENSP00000400676.1:p.Arg50His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1153C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.149G>A
  hgvsp: ENSP00000359181.3:p.Arg50His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.149G>A
  hgvsp: ENSP00000359188.1:p.Arg50His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-116G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1123G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1123G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.149G>A
  hgvsp: ENSP00000400517.1:p.Arg50His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-116G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1123G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.59G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1153C>T
  variant of: http://identifiers.org/hgnc/24542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg50His
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

10-103345881-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345881
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345881
    reference: chr 10
allele count: 4
allele frequency: 3.366946684399253e-5
allele num: 118802
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.148C>T
  hgvsp: ENSP00000359181.3:p.Arg50Cys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.148C>T
  hgvsp: ENSP00000299206.4:p.Arg50Cys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.148C>T
  hgvsp: ENSP00000400676.1:p.Arg50Cys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1152G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.148C>T
  hgvsp: ENSP00000414293.1:p.Arg50Cys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.148C>T
  hgvsp: ENSP00000359188.1:p.Arg50Cys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1122C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.72C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1122C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.58C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-117C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.181C>T
  hgvsp: ENSP00000411678.1:p.Arg61Cys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1152G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.148C>T
  hgvsp: ENSP00000400517.1:p.Arg50Cys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-117C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1122C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-117C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1122C>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg50Cys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

10-103345884-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345884
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345884
    reference: chr 10
allele count: 2
allele frequency: 1.688618709895306e-5
allele num: 118440
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.145G>A
  hgvsp: ENSP00000359188.1:p.Val49Met
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.145G>A
  hgvsp: ENSP00000299206.4:p.Val49Met
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1119G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.145G>A
  hgvsp: ENSP00000400676.1:p.Val49Met
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.69G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-120G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.145G>A
  hgvsp: ENSP00000359181.3:p.Val49Met
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-120G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.145G>A
  hgvsp: ENSP00000414293.1:p.Val49Met
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1119G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-120G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.178G>A
  hgvsp: ENSP00000411678.1:p.Val60Met
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1119G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1119G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.55G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1149C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.145G>A
  hgvsp: ENSP00000400517.1:p.Val49Met
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1149C>T
  variant of: http://identifiers.org/hgnc/24542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val49Met
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

10-103345891-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345891
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345891
    reference: chr 10
allele count: 1
allele frequency: 8.476587664869631e-6
allele num: 117972
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.62C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.138C>T
  hgvsp: ENST00000430045.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1142G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-127C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.138C>T
  hgvsp: ENST00000370162.3:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.171C>T
  hgvsp: ENST00000426919.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.138C>T
  hgvsp: ENST00000299206.4:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-127C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.138C>T
  hgvsp: ENST00000415897.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1112C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.138C>T
  hgvsp: ENST00000370169.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1112C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1142G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.48C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1112C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.138C>T
  hgvsp: ENST00000413344.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-127C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1112C>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala46Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

10-103345893-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345893
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345893
    reference: chr 10
allele count: 1
allele frequency: 8.482627578718784e-6
allele num: 117888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1140C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.136G>A
  hgvsp: ENSP00000359188.1:p.Ala46Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1110G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-129G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.46G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.60G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.136G>A
  hgvsp: ENSP00000400517.1:p.Ala46Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.136G>A
  hgvsp: ENSP00000400676.1:p.Ala46Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-129G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.169G>A
  hgvsp: ENSP00000411678.1:p.Ala57Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1110G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.136G>A
  hgvsp: ENSP00000299206.4:p.Ala46Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1110G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.136G>A
  hgvsp: ENSP00000414293.1:p.Ala46Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1110G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.136G>A
  hgvsp: ENSP00000359181.3:p.Ala46Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1140C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-129G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala46Thr
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

10-103345895-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345895
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345895
    reference: chr 10
allele count: 15
allele frequency: 1.274123403098668e-4
allele num: 117728
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1138C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.167G>A
  hgvsp: ENSP00000411678.1:p.Arg56Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1108G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.134G>A
  hgvsp: ENSP00000414293.1:p.Arg45Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-131G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1108G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.134G>A
  hgvsp: ENSP00000400517.1:p.Arg45Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.134G>A
  hgvsp: ENSP00000359181.3:p.Arg45Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.134G>A
  hgvsp: ENSP00000400676.1:p.Arg45Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-131G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.134G>A
  hgvsp: ENSP00000299206.4:p.Arg45Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.134G>A
  hgvsp: ENSP00000359188.1:p.Arg45Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.58G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.44G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1138C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1108G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1108G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-131G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg45Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

10-103345896-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345896
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345896
    reference: chr 10
allele count: 15
allele frequency: 1.274556454353885e-4
allele num: 117688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.133C>T
  hgvsp: ENSP00000359188.1:p.Arg45Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1107C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.133C>T
  hgvsp: ENSP00000414293.1:p.Arg45Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-132C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.133C>T
  hgvsp: ENSP00000400676.1:p.Arg45Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.133C>T
  hgvsp: ENSP00000299206.4:p.Arg45Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1107C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-132C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1137G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1137G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.57C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.133C>T
  hgvsp: ENSP00000400517.1:p.Arg45Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.166C>T
  hgvsp: ENSP00000411678.1:p.Arg56Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.43C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.133C>T
  hgvsp: ENSP00000359181.3:p.Arg45Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1107C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1107C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-132C>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg45Trp
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

10-103345898-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345898
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345898
    reference: chr 10
allele count: 1
allele frequency: 8.50933474021001e-6
allele num: 117518
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-134T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.131T>C
  hgvsp: ENSP00000359188.1:p.Leu44Pro
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.164T>C
  hgvsp: ENSP00000411678.1:p.Leu55Pro
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1105T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-134T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.131T>C
  hgvsp: ENSP00000400517.1:p.Leu44Pro
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.131T>C
  hgvsp: ENSP00000414293.1:p.Leu44Pro
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1105T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.41T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1135A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1135A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1105T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.131T>C
  hgvsp: ENSP00000299206.4:p.Leu44Pro
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.131T>C
  hgvsp: ENSP00000400676.1:p.Leu44Pro
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.131T>C
  hgvsp: ENSP00000359181.3:p.Leu44Pro
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-134T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.55T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1105T>C
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu44Pro
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

10-103345904-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345904
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345904
    reference: chr 10
allele count: 23
allele frequency: 1.964972234087997e-4
allele num: 117050
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.125G>A
  hgvsp: ENSP00000414293.1:p.Ser42Asn
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.125G>A
  hgvsp: ENSP00000400517.1:p.Ser42Asn
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.158G>A
  hgvsp: ENSP00000411678.1:p.Ser53Asn
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-140G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.125G>A
  hgvsp: ENSP00000299206.4:p.Ser42Asn
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.125G>A
  hgvsp: ENSP00000400676.1:p.Ser42Asn
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-140G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1099G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1129C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1099G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.125G>A
  hgvsp: ENSP00000359188.1:p.Ser42Asn
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.125G>A
  hgvsp: ENSP00000359181.3:p.Ser42Asn
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.35G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1099G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.49G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1099G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-140G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1129C>T
  variant of: http://identifiers.org/hgnc/24542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser42Asn
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

10-103345913-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345913
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345913
    reference: chr 10
allele count: 4
allele frequency: 3.433712186244549e-5
allele num: 116492
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.116A>G
  hgvsp: ENSP00000359181.3:p.Glu39Gly
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-149A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.116A>G
  hgvsp: ENSP00000400676.1:p.Glu39Gly
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-149A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.116A>G
  hgvsp: ENSP00000400517.1:p.Glu39Gly
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1090A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.116A>G
  hgvsp: ENSP00000299206.4:p.Glu39Gly
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1120T>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1090A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.116A>G
  hgvsp: ENSP00000359188.1:p.Glu39Gly
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1120T>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.116A>G
  hgvsp: ENSP00000414293.1:p.Glu39Gly
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.149A>G
  hgvsp: ENSP00000411678.1:p.Glu50Gly
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1090A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1090A>G
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu39Gly
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

10-103345915-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345915
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345915
    reference: chr 10
allele count: 1
allele frequency: 8.599043786330961e-6
allele num: 116292
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.116-2A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.149-2A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.116-2A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1118T>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-149-2A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.116-2A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1088A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-2A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.116-2A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-2A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-2A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.116-2A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-149-2A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.116-2A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1118T>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1088A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1088A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1088A>G
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.116-2A>G
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

10-103345919-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345919
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345919
    reference: chr 10
allele count: 16
allele frequency: 1.381931248920366e-4
allele num: 115780
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-6C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.116-6C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1084C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1084C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-149-6C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1084C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.116-6C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1084C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1114G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.116-6C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.116-6C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.116-6C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-6C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-149-6C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-6C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.116-6C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1114G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.149-6C>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34146
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.116-6C>T
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum

10-103345926-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345926
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345926
    reference: chr 10
allele count: 1
allele frequency: 8.747681864305959e-6
allele num: 114316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.116-13G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-13G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1077G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.149-13G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.116-13G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1077G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-13G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1077G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-13G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.116-13G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-149-13G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1107C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1077G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.116-13G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.116-13G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1107C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-149-13G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.116-13G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS

10-103345935-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345935
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345935
    reference: chr 10
allele count: 3
allele frequency: 2.892569951983339e-5
allele num: 103714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.116-22C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1098G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.149-22C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1098G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1068C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.116-22C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.116-22C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-22C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1068C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-149-22C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-22C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1068C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.116-22C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1068C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.116-22C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-149-22C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-22C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.116-22C>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/10-103345939-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345939
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345940
    reference: chr 10
allele count: 1
allele frequency: 9.786076370539996e-6
allele num: 102186
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1093dupC
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.116-27dupG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1063dupG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-149-27dupG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1063dupG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.116-27dupG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.116-27dupG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.116-27dupG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-149-27dupG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1063dupG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1093dupC
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.116-27dupG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-27dupG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-27dupG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1063dupG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.149-27dupG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.116-27dupG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-27dupG
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5664
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

10-103345940-CTGTTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345940
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345935
    reference: chr 10
allele count: 25792
allele frequency: 2.28086310576583e-1
allele num: 113080
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.116-32_116-28delCAACA
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-32_-149-28delCAACA
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1091_440-1087delGTTGT
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-32_26-28delCAACA
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.116-32_116-28delCAACA
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.116-32_116-28delCAACA
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1091_-176-1087delGTTGT
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1058_66+1062delCAACA
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.116-32_116-28delCAACA
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.116-32_116-28delCAACA
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1058_60+1062delCAACA
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-149-32_-149-28delCAACA
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-32_40-28delCAACA
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.149-32_149-28delCAACA
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.116-32_116-28delCAACA
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1058_60+1062delCAACA
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1058_60+1062delCAACA
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-149-32_-149-28delCAACA
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3198
  bin: 4.25e1
  variant carriers: 3026
genotype depth: GenotypeDepth
  all individuals: 9959
  bin: 2.75e1
  variant carriers: 2731
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 2.5e0
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 7.5e0
  variant carriers: 567
genotype depth: GenotypeDepth
  all individuals: 5712
  bin: 3.25e1
  variant carriers: 3480
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 5.25e1
  variant carriers: 1370
genotype quality: GenotypeQuality
num of homozygotes: 3054
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: CTGTTG
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

10-103345942-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345942
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345942
    reference: chr 10
allele count: 2
allele frequency: 2.786524368155599e-5
allele num: 71774
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-29C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.116-29C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-29C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-149-29C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1091G>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.116-29C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-149-29C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-29C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1061C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.116-29C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.116-29C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1061C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1061C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1061C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.116-29C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1091G>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.116-29C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.149-29C>G
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19027
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7437
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP

10-103345943-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345943
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345943
    reference: chr 10
allele count: 7
allele frequency: 1.040923150130859e-4
allele num: 67248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.116-30A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-30A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-149-30A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-149-30A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.116-30A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-30A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-30A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1090T>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.116-30A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1090T>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.116-30A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1060A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.116-30A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.149-30A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1060A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1060A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.116-30A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1060A>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

10-103345951-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345951
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345951
    reference: chr 10
allele count: 2
allele frequency: 1.817487868268479e-5
allele num: 110042
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.116-38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.116-38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1052A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.149-38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-149-38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1052A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.116-38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1082T>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1052A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.116-38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.116-38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1052A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-149-38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.116-38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1082T>A
  variant of: http://identifiers.org/hgnc/24542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6737
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17607
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

10-103345956-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345956
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345956
    reference: chr 10
allele count: 2
allele frequency: 1.829390995737519e-5
allele num: 109326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.116-43T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1047T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.116-43T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1047T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1047T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.116-43T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-43T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.116-43T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1077A>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-149-43T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-43T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.116-43T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1077A>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1047T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-43T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.116-43T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.149-43T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-149-43T>A
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9662
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-103345963-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103345963
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103345963
    reference: chr 10
allele count: 1
allele frequency: 9.325922333718804e-6
allele num: 107228
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.116-50A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.149-50A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1040A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1040A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.116-50A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.116-50A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-149-50A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1040A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.116-50A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-149-50A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-1070T>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1040A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.116-50A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-50A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.116-50A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-50A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-50A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-1070T>C
  variant of: http://identifiers.org/hgnc/24542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP

10-103346851-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346851
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346851
    reference: chr 10
allele count: 1
allele frequency: 8.367780697203488e-6
allele num: 119506
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+152C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+152C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-182G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-938C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+152C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+152C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-182G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-938C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+152C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+152C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-150+28C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+152C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+152C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-150+28C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.148+28C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+152C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-938C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+152C>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22440
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

10-103346868-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346868
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346868
    reference: chr 10
allele count: 4
allele frequency: 3.320438962030781e-5
allele num: 120466
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-150+11A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+135A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-165T>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-955A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+135A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-165T>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-955A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+135A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+135A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+135A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.148+11A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-150+11A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+135A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+135A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+135A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+135A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-955A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+135A>G
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/10-103346870-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346870
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346870
    reference: chr 10
allele count: 1
allele frequency: 8.296689620841284e-6
allele num: 120530
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+133G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+133G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-150+9G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-150+9G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-163C>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+133G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-957G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-957G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+133G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+133G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+133G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-163C>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.148+9G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+133G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+133G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+133G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+133G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-957G>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum

10-103346870-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346870
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346870
    reference: chr 10
allele count: 4
allele frequency: 3.318675848336514e-5
allele num: 120530
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+133G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-163C>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+133G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-957G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+133G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+133G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-163C>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-957G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.148+9G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+133G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-150+9G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+133G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-150+9G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-957G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+133G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+133G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+133G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+133G>C
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-103346875-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346875
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346875
    reference: chr 10
allele count: 1
allele frequency: 8.284866862189524e-6
allele num: 120702
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+128T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+128T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+128T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+128T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+128T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+128T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+128T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-150+4T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-158A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-158A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-150+4T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+128T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-962T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.148+4T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+128T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-962T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+128T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-962T>C
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29535
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.-150+4T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-103346881-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346881
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346881
    reference: chr 10
allele count: 1
allele frequency: 8.270751315049459e-6
allele num: 120908
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+122C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+122C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+122C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.146C>G
  hgvsp: ENSP00000411678.1:p.Ala49Gly
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-968C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-152C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+122C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-968C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+122C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-152C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-152G>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-968C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+122C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+122C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+122C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+122C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-152G>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+122C>G
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala49Gly
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP

10-103346886-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346886
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346886
    reference: chr 10
allele count: 4
allele frequency: 3.304965710980749e-5
allele num: 121030
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-147C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-973G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-973G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+117G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.141G>A
  hgvsp: ENST00000426919.1:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+117G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+117G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+117G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+117G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+117G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+117G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+117G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-157G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+117G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-157G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+117G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-973G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-147C>T
  variant of: http://identifiers.org/hgnc/24542
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly47Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-103346893-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346893
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346893
    reference: chr 10
allele count: 1
allele frequency: 8.254366559910193e-6
allele num: 121148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+110G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-164G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+110G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+110G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.134G>T
  hgvsp: ENSP00000411678.1:p.Cys45Phe
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+110G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+110G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-980G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-980G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-140C>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+110G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+110G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-164G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+110G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+110G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-140C>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-980G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+110G>T
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys45Phe
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

10-103346902-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346902
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346902
    reference: chr 10
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-173A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+101A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-131T>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+101A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+101A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+101A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+101A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-131T>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-989A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+101A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+101A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-989A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.125A>C
  hgvsp: ENSP00000411678.1:p.Asp42Ala
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-173A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+101A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+101A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-989A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+101A>C
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp42Ala
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

10-103346905-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346905
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346905
    reference: chr 10
allele count: 2
allele frequency: 1.648532805802836e-5
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+98C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+98C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+98C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-176C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+98C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-992C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+98C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-992C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+98C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.122C>T
  hgvsp: ENSP00000411678.1:p.Ala41Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+98C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-176C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-128G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+98C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+98C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+98C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-992C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-128G>A
  variant of: http://identifiers.org/hgnc/24542
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala41Val
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

10-103346908-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346908
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346908
    reference: chr 10
allele count: 2
allele frequency: 1.64836976230508e-5
allele num: 121332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-179G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+95G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+95G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-995G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+95G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+95G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-125C>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+95G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-995G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+95G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+95G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+95G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-995G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.119G>C
  hgvsp: ENSP00000411678.1:p.Gly40Ala
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-125C>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-179G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+95G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+95G>C
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly40Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

10-103346910-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346910
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346910
    reference: chr 10
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-181T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+93T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+93T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+93T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+93T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-997T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+93T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.117T>C
  hgvsp: ENST00000426919.1:c.117T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-181T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-123A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+93T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-997T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+93T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+93T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-123A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+93T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+93T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-997T>C
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24393
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile39Ile
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ

10-103346911-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346911
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346911
    reference: chr 10
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+92T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+92T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-998T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+92T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+92T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-122A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+92T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.116T>C
  hgvsp: ENSP00000411678.1:p.Ile39Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-182T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+92T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+92T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-182T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+92T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-122A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-998T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+92T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-998T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+92T>C
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile39Thr
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

10-103346926-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346926
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346926
    reference: chr 10
allele count: 4
allele frequency: 3.295327225993541e-5
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+77G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-107C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-1013G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-197G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-1013G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+77G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.101G>A
  hgvsp: ENSP00000411678.1:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-1013G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+77G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-107C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+77G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-197G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+77G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+77G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+77G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+77G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+77G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+77G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Cys34Tyr
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

10-103346935-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346935
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346935
    reference: chr 10
allele count: 17
allele frequency: 1.400444847186754e-4
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-1022G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-98C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-1022G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-206G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+68G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.92G>A
  hgvsp: ENSP00000411678.1:p.Arg31His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+68G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+68G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+68G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+68G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-98C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+68G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+68G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+68G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+68G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-206G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+68G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-1022G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
hgvs: p.Arg31His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

10-103346936-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346936
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346936
    reference: chr 10
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.91C>T
  hgvsp: ENSP00000411678.1:p.Arg31Cys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-149-1023C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-207C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+67C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-97G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+67C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-207C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+67C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+67C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+67C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+67C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-97G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+67C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.40-1023C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+67C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.26-1023C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+67C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+67C>T
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg31Cys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

10-103346952-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346952
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346952
    reference: chr 10
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+51A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-150+1009A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+51A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390093
  ensembl transcript: ENST00000454524
  gene symbol: POLL
  hgvsc: ENST00000454524.1:c.-223A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+51A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.75A>C
  hgvsp: ENST00000426919.1:c.75A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-223A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.39+1009A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+51A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+51A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+51A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-81T>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+51A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+51A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-81T>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.25+1009A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+51A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+51A>C
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser25Ser
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

10-103346959-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346959
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346959
    reference: chr 10
allele count: 13
allele frequency: 1.070822556465297e-4
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+44A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+44A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+44A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-228-2A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+44A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-74T>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-150+1002A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.25+1002A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.70-2A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+44A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+44A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+44A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+44A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-74T>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.39+1002A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+44A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+44A>T
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.-228-2A>T
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

10-103346965-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346965
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346965
    reference: chr 10
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.25+996A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.70-8A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-150+996A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-68T>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-228-8A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-68T>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+38A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.39+996A>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+38A>T
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.-228-8A>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

10-103346974-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346974
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346974
    reference: chr 10
allele count: 3
allele frequency: 2.471088267272907e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+29T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.70-17T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+29T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+29T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+29T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-59A>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+29T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+29T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+29T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+29T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+29T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.39+987T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-150+987T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+29T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-59A>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.25+987T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-228-17T>A
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

10-103346976-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346976
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346976
    reference: chr 10
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+27C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+27C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+27C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-57G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-57G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-228-19C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+27C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+27C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+27C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.39+985C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+27C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.70-19C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-150+985C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.25+985C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+27C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+27C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+27C>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

10-103346979-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346979
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346979
    reference: chr 10
allele count: 3
allele frequency: 2.471088267272907e-5
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.70-22C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+24C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.39+982C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+24C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-150+982C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+24C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+24C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+24C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.25+982C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+24C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+24C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-54G>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+24C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-54G>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+24C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-228-22C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+24C>G
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

10-103346996-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346996
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346996
    reference: chr 10
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.25+965T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+7T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+7T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+7T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-150+965T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-37A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.70-39T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+7T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-228-39T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+7T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+7T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+7T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-37A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+7T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.39+965T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+7T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+7T>C
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.115+7T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

10-103346999-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103346999
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103346999
    reference: chr 10
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+4A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+4A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-150+962A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-228-42A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+4A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.25+962A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+4A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+4A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+4A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+4A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-34T>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+4A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+4A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+4A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-34T>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.70-42A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.39+962A>G
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.115+4A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

10-103347000-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103347000
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103347000
    reference: chr 10
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+3G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-33C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+3G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+3G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-150+961G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-228-43G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+3G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+3G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.70-43G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+3G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+3G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+3G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.25+961G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+3G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+3G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-33C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.39+961G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.115+3G>A
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

10-103347002-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103347002
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103347002
    reference: chr 10
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.70-45G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.115+1G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.115+1G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.115+1G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.115+1G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.115+1G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.115+1G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.60+1G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.60+1G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.60+1G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-150+959G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-31C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.66+1G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-31C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-228-45G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.25+959G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.39+959G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.115+1G>A
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum

10-103347012-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103347012
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103347012
    reference: chr 10
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.106G>A
  hgvsp: ENSP00000359181.3:p.Glu36Lys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.106G>A
  hgvsp: ENSP00000359188.1:p.Glu36Lys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.106G>A
  hgvsp: ENSP00000400517.1:p.Glu36Lys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.106G>A
  hgvsp: ENSP00000299206.4:p.Glu36Lys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-21C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.51G>A
  hgvsp: ENST00000339310.3:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.69+37G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.106G>A
  hgvsp: ENSP00000414293.1:p.Glu36Lys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.51G>A
  hgvsp: ENST00000429502.1:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-228-55G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-150+949G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.25+949G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.106G>A
  hgvsp: ENSP00000400676.1:p.Glu36Lys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.57G>A
  hgvsp: ENST00000370158.3:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.51G>A
  hgvsp: ENST00000456836.2:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-21C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.39+949G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5672
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu36Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

10-103347019-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103347019
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103347019
    reference: chr 10
allele count: 4
allele frequency: 3.29489291598023e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.44G>A
  hgvsp: ENSP00000406791.1:p.Arg15Lys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.69+30G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.44G>A
  hgvsp: ENSP00000343102.3:p.Arg15Lys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.99G>A
  hgvsp: ENST00000370169.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-14C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.99G>A
  hgvsp: ENST00000413344.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.99G>A
  hgvsp: ENST00000415897.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.39+942G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-228-62G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.50G>A
  hgvsp: ENSP00000359177.3:p.Arg17Lys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.44G>A
  hgvsp: ENSP00000390810.2:p.Arg15Lys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.99G>A
  hgvsp: ENST00000370162.3:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.99G>A
  hgvsp: ENST00000430045.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.99G>A
  hgvsp: ENST00000299206.4:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-14C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.25+942G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-150+942G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg15Lys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

10-103347028-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103347028
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103347028
    reference: chr 10
allele count: 4
allele frequency: 3.29489291598023e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.90G>A
  hgvsp: ENST00000413344.1:c.90G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.35G>A
  hgvsp: ENSP00000406791.1:p.Gly12Glu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.90G>A
  hgvsp: ENST00000370169.1:c.90G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176-5C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.90G>A
  hgvsp: ENST00000415897.1:c.90G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.39+933G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.90G>A
  hgvsp: ENST00000299206.4:c.90G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.25+933G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.69+21G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.35G>A
  hgvsp: ENSP00000343102.3:p.Gly12Glu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.41G>A
  hgvsp: ENSP00000359177.3:p.Gly14Glu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440-5C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.35G>A
  hgvsp: ENSP00000390810.2:p.Gly12Glu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.90G>A
  hgvsp: ENST00000430045.1:c.90G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.90G>A
  hgvsp: ENST00000370162.3:c.90G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-228-71G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-150+933G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly12Glu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

10-103347033-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103347033
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103347033
    reference: chr 10
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.30C>T
  hgvsp: ENST00000429502.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.69+16C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.25+928C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-150+928C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.85C>T
  hgvsp: ENSP00000400517.1:p.Pro29Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.85C>T
  hgvsp: ENSP00000400676.1:p.Pro29Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.440G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.85C>T
  hgvsp: ENSP00000414293.1:p.Pro29Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.85C>T
  hgvsp: ENSP00000359181.3:p.Pro29Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-176G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.85C>T
  hgvsp: ENSP00000359188.1:p.Pro29Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.30C>T
  hgvsp: ENST00000339310.3:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.85C>T
  hgvsp: ENSP00000299206.4:p.Pro29Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.39+928C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.30C>T
  hgvsp: ENST00000456836.2:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-228-76C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.36C>T
  hgvsp: ENST00000370158.3:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro29Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

10-103347035-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103347035
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103347035
    reference: chr 10
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.83T>C
  hgvsp: ENSP00000299206.4:p.Ile28Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.25+926T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.28T>C
  hgvsp: ENSP00000390810.2:p.Phe10Leu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.69+14T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.83T>C
  hgvsp: ENSP00000359188.1:p.Ile28Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.28T>C
  hgvsp: ENSP00000406791.1:p.Phe10Leu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-228-78T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.83T>C
  hgvsp: ENSP00000414293.1:p.Ile28Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.442A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.83T>C
  hgvsp: ENSP00000359181.3:p.Ile28Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.83T>C
  hgvsp: ENSP00000400676.1:p.Ile28Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.34T>C
  hgvsp: ENSP00000359177.3:p.Phe12Leu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.28T>C
  hgvsp: ENSP00000343102.3:p.Phe10Leu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.83T>C
  hgvsp: ENSP00000400517.1:p.Ile28Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-174A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-150+926T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.39+926T>C
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile28Thr
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ

10-103347053-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103347053
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103347053
    reference: chr 10
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.65C>G
  hgvsp: ENSP00000359188.1:p.Ser22Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-156G>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.65C>G
  hgvsp: ENSP00000411678.1:p.Ser22Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.10C>G
  hgvsp: ENSP00000343102.3:p.Gln4Glu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.65C>G
  hgvsp: ENSP00000414293.1:p.Ser22Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.39+908C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.65C>G
  hgvsp: ENSP00000400517.1:p.Ser22Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.10C>G
  hgvsp: ENSP00000406791.1:p.Gln4Glu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.10C>G
  hgvsp: ENSP00000390810.2:p.Gln4Glu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-228-96C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.65C>G
  hgvsp: ENSP00000359181.3:p.Ser22Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-150+908C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.65C>G
  hgvsp: ENSP00000299206.4:p.Ser22Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.460G>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.65C>G
  hgvsp: ENSP00000400676.1:p.Ser22Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.25+908C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.16C>G
  hgvsp: ENSP00000359177.3:p.Gln6Glu
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser22Ter
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-103347058-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103347058
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103347058
    reference: chr 10
allele count: 25
allele frequency: 2.059308072487644e-4
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.60A>G
  hgvsp: ENST00000299206.4:c.60A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.60A>G
  hgvsp: ENST00000426919.1:c.60A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.60A>G
  hgvsp: ENST00000430045.1:c.60A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.60A>G
  hgvsp: ENST00000413344.1:c.60A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-151T>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.5A>G
  hgvsp: ENSP00000343102.3:p.His2Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.465T>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.60A>G
  hgvsp: ENST00000370162.3:c.60A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.39+903A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.5A>G
  hgvsp: ENSP00000390810.2:p.His2Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.5A>G
  hgvsp: ENSP00000406791.1:p.His2Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.11A>G
  hgvsp: ENSP00000359177.3:p.His4Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.60A>G
  hgvsp: ENST00000370169.1:c.60A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-228-101A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.60A>G
  hgvsp: ENST00000415897.1:c.60A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-150+903A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.25+903A>G
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His2Arg
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/10-103347061-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103347061
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103347061
    reference: chr 10
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000414293
  ensembl transcript: ENST00000430045
  gene symbol: POLL
  hgvsc: ENST00000430045.1:c.57T>G
  hgvsp: ENSP00000414293.1:p.Asp19Glu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.57T>G
  hgvsp: ENSP00000299206.4:p.Asp19Glu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.468A>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000405331
  ensembl transcript: ENST00000436284
  gene symbol: POLL
  hgvsc: ENST00000436284.2:c.-150+900T>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.57T>G
  hgvsp: ENSP00000359181.3:p.Asp19Glu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.8T>G
  hgvsp: ENSP00000359177.3:p.Met3Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.57T>G
  hgvsp: ENSP00000359188.1:p.Asp19Glu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.2T>G
  hgvsp: ENSP00000406791.1:p.Met1?
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.2T>G
  hgvsp: ENSP00000343102.3:p.Met1?
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.2T>G
  hgvsp: ENSP00000390810.2:p.Met1?
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.57T>G
  hgvsp: ENSP00000400676.1:p.Asp19Glu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.-228-104T>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-148A>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.25+900T>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000411678
  ensembl transcript: ENST00000426919
  gene symbol: POLL
  hgvsc: ENST00000426919.1:c.57T>G
  hgvsp: ENSP00000411678.1:p.Asp19Glu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400517
  ensembl transcript: ENST00000413344
  gene symbol: POLL
  hgvsc: ENST00000413344.1:c.57T>G
  hgvsp: ENSP00000400517.1:p.Asp19Glu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000461587
  gene symbol: POLL
  hgvsc: ENST00000461587.1:n.39+900T>G
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

GenotypeDepth
all individuals: 4617
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38741
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 396
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 354
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 40
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 474
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 905
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 17
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14030
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5956
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1318
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48200
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 790
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 889
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1468
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515472979116782e-5
allele num: 65986
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.51e0

FS
type: SiteQuality
SIO_000300: 1.243e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

QD
type: SiteQuality
SIO_000300: 1.591e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.32e-1

MQ
type: SiteQuality
SIO_000300: 5.735e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e-1

DP
type: SiteQuality
SIO_000300: 1.455727e6

GenotypeDepth
all individuals: 41
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 55
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 399
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 510
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 656
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 351
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38665
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 82
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 906
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5961
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 790
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48185
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1320
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1474
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65936
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

QD
type: SiteQuality
SIO_000300: 1.162e1

FS
type: SiteQuality
SIO_000300: 1.408e0

DP
type: SiteQuality
SIO_000300: 1.454564e6

MQ
type: SiteQuality
SIO_000300: 5.971e1

MQRankSum
type: SiteQuality
SIO_000300: 7.0e-3

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38292
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 13808
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 682
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4653
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 949
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 353
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1470
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47504
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1387
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 5943
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 7.5e0
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.587253414264037e-4
allele num: 6590
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.86e0

DP
type: SiteQuality
SIO_000300: 1.448206e6

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.052e0

QD
type: SiteQuality
SIO_000300: 1.309e1

FS
type: SiteQuality
SIO_000300: 5.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

GenotypeDepth
all individuals: 433
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 937
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13818
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 38199
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47343
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1468
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 232
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1320
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5916
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524762137106611e-5
allele num: 65584
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.978630787495053e-4
allele num: 10108
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.069434328720563e-5
allele num: 16476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.25e-1

QD
type: SiteQuality
SIO_000300: 1.38e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 1.447964e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 977
bin: 1.25e1
variant carriers: 3

GenotypeDepth
all individuals: 4650
bin: 3.25e1
variant carriers: 10

GenotypeDepth
all individuals: 61
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 38098
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 368
bin: 4.25e1
variant carriers: 12

GenotypeDepth
all individuals: 942
bin: 3.75e1
variant carriers: 13

GenotypeDepth
all individuals: 15
bin: 8.75e1
variant carriers: 2

GenotypeDepth
all individuals: 20
bin: 8.25e1
variant carriers: 3

GenotypeDepth
all individuals: 24
bin: 7.25e1
variant carriers: 3

GenotypeDepth
all individuals: 13831
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 720
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 28
bin: 7.75e1
variant carriers: 3

GenotypeDepth
all individuals: 70
bin: 6.75e1
variant carriers: 15

GenotypeDepth
all individuals: 193
bin: 4.75e1
variant carriers: 15

GenotypeDepth
all individuals: 96
bin: 5.75e1
variant carriers: 15

GenotypeQuality
all individuals: 1451
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 9.75e1
variant carriers: 139

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47420
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5894
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1462
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1316
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 249
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 6
allele frequency: 5.198405822214521e-4
allele num: 11542
num of homozygotes: 0

South Asian
type: Population
allele count: 33
allele frequency: 2.002670226969293e-3
allele num: 16478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.967359050445104e-4
allele num: 10110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.035822707953856e-4
allele num: 6588
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.118568232662192e-3
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 95
allele frequency: 1.448877501220107e-3
allele num: 65568
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

DP
type: SiteQuality
SIO_000300: 1.452439e6

MQRankSum
type: SiteQuality
SIO_000300: 5.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.6e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.96e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

QD
type: SiteQuality
SIO_000300: 1.289e1

GenotypeDepth
all individuals: 95
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 365
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4679
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 943
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37969
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 802
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 366
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13826
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 83
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1093
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 58
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 28
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1470
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 5941
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1320
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1648
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47424
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.056701818737582e-5
allele num: 65430
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.076810889645114e-5
allele num: 16456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.162790697674419e-4
allele num: 8600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10064
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

QD
type: SiteQuality
SIO_000300: 1.213e1

DP
type: SiteQuality
SIO_000300: 1.446752e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

GenotypeDepth
all individuals: 23
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 946
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 363
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 25
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 974
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 181
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 29
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1254
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 362
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13700
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47171
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1957
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1457
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1316
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5910
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.818012566907144e-4
allele num: 8594
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9976
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65118
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.440729e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.133e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQ
type: SiteQuality
SIO_000300: 5.941e1

VQSLOD
type: SiteQuality
SIO_000300: 4.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e-1

QD
type: SiteQuality
SIO_000300: 1.003e1

MQRankSum
type: SiteQuality
SIO_000300: -4.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-2

FS
type: SiteQuality
SIO_000300: 4.069e0

GenotypeDepth
all individuals: 58
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1303
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13659
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 29
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 182
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 392
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4700
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 183
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 41
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37543
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 368
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5895
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46953
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2014
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 210
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1301
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.222792858889704e-4
allele num: 16356
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.163602513381429e-4
allele num: 8594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.53817756721836e-5
allele num: 65012
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.674531575294934e-5
allele num: 11528
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9930
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.8e-1

QD
type: SiteQuality
SIO_000300: 1.22e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.18e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

DP
type: SiteQuality
SIO_000300: 1.439019e6

GenotypeDepth
all individuals: 42
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 27
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 13644
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 374
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4692
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37444
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1352
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1051
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 955
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 185
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 407
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 795
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 5887
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2050
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1299
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1439
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46786
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.117704637220115e-5
allele num: 16346
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.734906315058987e-4
allele num: 11528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539835545563734e-5
allele num: 64942
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9912
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.31e-1

QD
type: SiteQuality
SIO_000300: 1.097e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

FS
type: SiteQuality
SIO_000300: 2.959e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

DP
type: SiteQuality
SIO_000300: 1.437953e6

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

GenotypeDepth
all individuals: 267
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13648
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 466
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1371
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 180
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 94
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 367
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4682
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 17
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37243
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1439
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46608
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5886
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1291
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 639
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2051
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9812
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.329373398555789e-4
allele num: 8586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64742
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16290
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.15e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.073e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

VQSLOD
type: SiteQuality
SIO_000300: 2.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

DP
type: SiteQuality
SIO_000300: 1.434299e6

GenotypeDepth
all individuals: 1315
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 953
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 343
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1442
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 581
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36928
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4663
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1292
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2342
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1436
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5829
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46160
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9706
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.679048776254123e-5
allele num: 11522
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16200
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.59e-1

QD
type: SiteQuality
SIO_000300: 7.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.99e-1

FS
type: SiteQuality
SIO_000300: 9.6e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.667e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.66e-1

MQ
type: SiteQuality
SIO_000300: 5.615e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

DP
type: SiteQuality
SIO_000300: 1.428363e6

GenotypeDepth
all individuals: 959
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36823
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13497
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4672
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 350
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1361
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1481
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 377
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 183
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2453
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5792
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 152
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46090
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1274
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.165772907437631e-4
allele num: 8578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64448
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16168
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9698
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.914e1

VQSLOD
type: SiteQuality
SIO_000300: 4.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.862e0

QD
type: SiteQuality
SIO_000300: 1.175e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.63e-1

DP
type: SiteQuality
SIO_000300: 1.427429e6

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-1

GenotypeDepth
all individuals: 385
bin: 4.25e1
variant carriers: 2

GenotypeDepth
all individuals: 25
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1409
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 43
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 58
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 100
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4668
bin: 3.25e1
variant carriers: 3

GenotypeDepth
all individuals: 374
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 967
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 610
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 25
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36737
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 13448
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 29
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 87
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5774
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1268
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1415
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2491
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 467
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45966
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 128
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 14
allele frequency: 1.451077943615257e-3
allele num: 9648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.680555555555556e-5
allele num: 11520
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.654e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

FS
type: SiteQuality
SIO_000300: 1.121e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.135e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.426844e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

GenotypeDepth
all individuals: 378
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4656
bin: 3.25e1
variant carriers: 3

GenotypeDepth
all individuals: 620
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1429
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13442
bin: 2.75e1
variant carriers: 3

GenotypeDepth
all individuals: 98
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 968
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 42
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1512
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 36706
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 816
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2528
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5784
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45959
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1420
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1279
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

South Asian
type: Population
allele count: 13
allele frequency: 8.069522036002483e-4
allele num: 16110
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.332633543270352e-4
allele num: 8574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64378
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.425806e6

QD
type: SiteQuality
SIO_000300: 1.184e1

FS
type: SiteQuality
SIO_000300: 3.852e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.809e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.57e-1

GenotypeDepth
all individuals: 4641
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 17
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 681
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13377
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 195
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 385
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1467
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 410
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1620
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45635
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 790
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 631
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1419
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1271
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5748
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2651
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16050
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.555161581288296e-5
allele num: 64302
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.48e-1

DP
type: SiteQuality
SIO_000300: 1.422897e6

MQRankSum
type: SiteQuality
SIO_000300: 7.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

FS
type: SiteQuality
SIO_000300: 3.198e0

QD
type: SiteQuality
SIO_000300: 1.118e1

GenotypeDepth
all individuals: 30
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 511
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13227
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1759
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 99
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 65
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 220
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 428
bin: 4.25e1
variant carriers: 3

GenotypeDepth
all individuals: 36067
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1016
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 27
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4675
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 177
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1245
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 811
bin: 9.75e1
variant carriers: 22

GenotypeQuality
all individuals: 131
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45058
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5690
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2838
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1394
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 23
allele frequency: 3.588815378854076e-4
allele num: 64088
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15918
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.421996e6

FS
type: SiteQuality
SIO_000300: 2.762e0

VQSLOD
type: SiteQuality
SIO_000300: -7.72e-1

MQ
type: SiteQuality
SIO_000300: 5.403e1

QD
type: SiteQuality
SIO_000300: 9.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.354e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.942e0

GenotypeDepth
all individuals: 13074
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4721
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 160
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 570
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 345
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 938
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2074
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 533
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 34962
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1708
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1106
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 28
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5589
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 765
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1336
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1207
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3756
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44331
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.91107147407313e-4
allele num: 15698
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.058649163667161e-4
allele num: 9446
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.428058e6

VQSLOD
type: SiteQuality
SIO_000300: 9.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.84e-1

FS
type: SiteQuality
SIO_000300: 5.639999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.2e-2

QD
type: SiteQuality
SIO_000300: 1.3e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

GenotypeDepth
all individuals: 30
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1148
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34735
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1055
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4708
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2184
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 583
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 87
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 402
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 189
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 14
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5534
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43892
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4174
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1324
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1194
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.568578240682645e-5
allele num: 63752
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.348e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.811e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.070000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.406e1

MQ
type: SiteQuality
SIO_000300: 5.465e1

DP
type: SiteQuality
SIO_000300: 1.426327e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.69e-1

GenotypeDepth
all individuals: 22
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1240
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 2

GenotypeDepth
all individuals: 116
bin: 6.25e1
variant carriers: 4

GenotypeDepth
all individuals: 2391
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1206
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 15
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 627
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12706
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4678
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 242
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 25
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1817
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 5.75e1
variant carriers: 3

GenotypeDepth
all individuals: 611
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 40
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4743
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1291
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42895
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 800
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 5423
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1169
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.238344683080147e-4
allele num: 11454
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.469979296066253e-5
allele num: 15456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.260279151832131e-4
allele num: 63478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9404
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.149425287356322e-3
allele num: 870
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.08e-1

FS
type: SiteQuality
SIO_000300: 2.035e0

MQ
type: SiteQuality
SIO_000300: 5.897e1

MQRankSum
type: SiteQuality
SIO_000300: -1.5e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.125e-1

QD
type: SiteQuality
SIO_000300: 1.225e1

DP
type: SiteQuality
SIO_000300: 1.430073e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.97e0

GenotypeDepth
all individuals: 130
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 288
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1542
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4806
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 201
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12193
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 816
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 93
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5138
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1241
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6137
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1473
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39931
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62708
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.672894701721607e-5
allele num: 14986
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.45e-1

QD
type: SiteQuality
SIO_000300: 8.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.817e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

DP
type: SiteQuality
SIO_000300: 1.432896e6

FS
type: SiteQuality
SIO_000300: 1.255e0

GenotypeDepth
all individuals: 942
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10828
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 610
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2068
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5816
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 376
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25659
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 47
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3370
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 128
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2175
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1020
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1131
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1790
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2820
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2096
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5207
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1018
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1486
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1989
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1007
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3820
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30199
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8494
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55828
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5926
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.628928898382667e-5
allele num: 13108
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.822489520685256e-4
allele num: 10974
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.526626e6

MQRankSum
type: SiteQuality
SIO_000300: 6.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.37e-1

MQ
type: SiteQuality
SIO_000300: 5.917e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.711e0

VQSLOD
type: SiteQuality
SIO_000300: 2.15e0

QD
type: SiteQuality
SIO_000300: 1.094e1

GenotypeDepth
all individuals: 830
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1683
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1049
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 23735
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 189
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2150
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 443
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2906
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 18
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 133
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1142
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27131
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1219
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1087
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1933
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2227
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5023
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1654
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2957
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2446
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2090
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1005
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3661
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2270
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55138
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5886
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.160864785635764e-5
allele num: 10916
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e0

QD
type: SiteQuality
SIO_000300: 1.161e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.545188e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.004e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.800000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

MQ
type: SiteQuality
SIO_000300: 6.073e1

VQSLOD
type: SiteQuality
SIO_000300: 3.02e0

GenotypeDepth
all individuals: 2458
bin: 1.75e1
variant carriers: 1307

GenotypeDepth
all individuals: 344
bin: 6.75e1
variant carriers: 310

GenotypeDepth
all individuals: 861
bin: 5.75e1
variant carriers: 818

GenotypeDepth
all individuals: 3965
bin: 3.75e1
variant carriers: 3532

GenotypeDepth
all individuals: 191
bin: 7.75e1
variant carriers: 175

GenotypeDepth
all individuals: 545
bin: 6.25e1
variant carriers: 520

GenotypeDepth
all individuals: 93
bin: 8.75e1
variant carriers: 87

GenotypeDepth
all individuals: 4456
bin: 1.25e1
variant carriers: 1046

GenotypeDepth
all individuals: 75
bin: 9.25e1
variant carriers: 68

GenotypeDepth
all individuals: 20790
bin: 2.25e1
variant carriers: 1743

GenotypeDepth
all individuals: 339
bin: 9.75e1
variant carriers: 323

GenotypeDepth
all individuals: 234
bin: 7.25e1
variant carriers: 218

GenotypeDepth
all individuals: 129
bin: 8.25e1
variant carriers: 117

GenotypeDepth
all individuals: 2146
bin: 4.75e1
variant carriers: 2045

GenotypeQuality
all individuals: 275
bin: 5.75e1
variant carriers: 110

GenotypeQuality
all individuals: 238
bin: 4.25e1
variant carriers: 105

GenotypeQuality
all individuals: 210
bin: 4.75e1
variant carriers: 91

GenotypeQuality
all individuals: 1121
bin: 7.5e0
variant carriers: 56

GenotypeQuality
all individuals: 897
bin: 3.25e1
variant carriers: 81

GenotypeQuality
all individuals: 479
bin: 3.75e1
variant carriers: 102

GenotypeQuality
all individuals: 23620
bin: 6.25e1
variant carriers: 147

GenotypeQuality
all individuals: 233
bin: 1.75e1
variant carriers: 77

GenotypeQuality
all individuals: 845
bin: 7.75e1
variant carriers: 159

GenotypeQuality
all individuals: 3770
bin: 2.25e1
variant carriers: 79

GenotypeQuality
all individuals: 346
bin: 9.25e1
variant carriers: 189

GenotypeQuality
all individuals: 845
bin: 2.75e1
variant carriers: 97

GenotypeQuality
all individuals: 488
bin: 2.5e0
variant carriers: 42

GenotypeQuality
all individuals: 270
bin: 5.25e1
variant carriers: 116

GenotypeQuality
all individuals: 840
bin: 7.25e1
variant carriers: 128

GenotypeQuality
all individuals: 264
bin: 1.25e1
variant carriers: 98

GenotypeQuality
all individuals: 2901
bin: 6.75e1
variant carriers: 112

GenotypeQuality
all individuals: 519
bin: 8.25e1
variant carriers: 150

GenotypeQuality
all individuals: 21935
bin: 9.75e1
variant carriers: 21438

GenotypeQuality
all individuals: 313
bin: 8.75e1
variant carriers: 197

East Asian
type: Population
allele count: 276
allele frequency: 3.235638921453693e-2
allele num: 8530
num of homozygotes: 6

European (Finnish)
type: Population
allele count: 1619
allele frequency: 2.477050183598531e-1
allele num: 6536
num of homozygotes: 201

South Asian
type: Population
allele count: 2514
allele frequency: 1.764458169567659e-1
allele num: 14248
num of homozygotes: 262

European (Non-Finnish)
type: Population
allele count: 17896
allele frequency: 2.864001536344141e-1
allele num: 62486
num of homozygotes: 2340

African
type: Population
allele count: 1650
allele frequency: 1.830892143808256e-1
allele num: 9012
num of homozygotes: 119

Other
type: Population
allele count: 199
allele frequency: 2.330210772833724e-1
allele num: 854
num of homozygotes: 15

Latino
type: Population
allele count: 1638
allele frequency: 1.435079726651481e-1
allele num: 11414
num of homozygotes: 111

MQRankSum
type: SiteQuality
SIO_000300: -3.95e0

DP
type: SiteQuality
SIO_000300: 1.674025e6

MQ
type: SiteQuality
SIO_000300: 5.048e1

QD
type: SiteQuality
SIO_000300: 1.172e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-2

FS
type: SiteQuality
SIO_000300: 4.151e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.87e0

GenotypeDepth
all individuals: 1872
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3569
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 67
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1350
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 478
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 806
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3827
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 315
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2948
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23573
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8670
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3952
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.180661577608143e-4
allele num: 6288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34262
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10032
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8042
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 528
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-2

QD
type: SiteQuality
SIO_000300: 1.21e1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.63e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.23e0

FS
type: SiteQuality
SIO_000300: 4.168e0

MQ
type: SiteQuality
SIO_000300: 5.863e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.35e-1

DP
type: SiteQuality
SIO_000300: 8.88323e5

GenotypeDepth
all individuals: 7
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1120
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7022
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 12
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18349
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1898
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 450
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 177
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 880
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2724
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22357
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3771
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 9.75e1
variant carriers: 7

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.917790705107716e-4
allele num: 31286
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5916
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.196458482890644e-4
allele num: 8358
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7974
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3708
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 480
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.53e-1

QD
type: SiteQuality
SIO_000300: 1.033e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.81e-2

MQ
type: SiteQuality
SIO_000300: 5.962e1

FS
type: SiteQuality
SIO_000300: 8.070000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

DP
type: SiteQuality
SIO_000300: 7.83197e5

MQRankSum
type: SiteQuality
SIO_000300: -2.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.5e-1

GenotypeDepth
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 798
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12060
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8587
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1852
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6225
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3188
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4612
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1157
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2183
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1114
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26890
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6363
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1553
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1298
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2368
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 852
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3771
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11360
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8748
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.354603249352484e-4
allele num: 8494
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.88e-1

QD
type: SiteQuality
SIO_000300: 9.19e0

FS
type: SiteQuality
SIO_000300: 6.585e0

MQRankSum
type: SiteQuality
SIO_000300: 9.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.82e-1

DP
type: SiteQuality
SIO_000300: 1.359339e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 10522
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 64
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1865
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 162
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 778
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5922
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1864
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5935
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 33
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 851
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2480
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6020
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4385
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2342
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2090
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1553
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 304
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4351
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1274
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1432
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23848
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1764
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4439
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8724
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.263068589701755e-5
allele num: 61292
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12198
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.86e0

MQRankSum
type: SiteQuality
SIO_000300: 2.35e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.33168e6

QD
type: SiteQuality
SIO_000300: 1.307e1

FS
type: SiteQuality
SIO_000300: 1.699e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.186e0

GenotypeDepth
all individuals: 4547
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1680
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1854
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9879
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 162
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 376
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9527
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3034
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15104
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2373
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4129
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4718
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3170
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1244
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5576
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5750
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2495
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4745
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1443
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1552
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11272
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8400
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.170686022008897e-4
allele num: 8542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11266
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60538
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

VQSLOD
type: SiteQuality
SIO_000300: 2.43e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

MQRankSum
type: SiteQuality
SIO_000300: -9.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

FS
type: SiteQuality
SIO_000300: 4.191e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

QD
type: SiteQuality
SIO_000300: 1.015e1

DP
type: SiteQuality
SIO_000300: 1.309266e6

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 875
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1691
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 189
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 648
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1209
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1003
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 47999
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1052
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5571
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65644
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.089392278650591e-5
allele num: 16422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9928
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.27e-1

DP
type: SiteQuality
SIO_000300: 1.477922e6

MQRankSum
type: SiteQuality
SIO_000300: -1.782e0

FS
type: SiteQuality
SIO_000300: 4.314e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.586e0

VQSLOD
type: SiteQuality
SIO_000300: -1.332e0

QD
type: SiteQuality
SIO_000300: 1.731e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 193
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 149
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 663
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23636
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 454
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 128
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50397
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5736
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1007
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 9.75e1
variant carriers: 4

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66166
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.472222222222222e-4
allele num: 11520
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.3e0

FS
type: SiteQuality
SIO_000300: 2.864e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.183e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.33e-1

QD
type: SiteQuality
SIO_000300: 1.53e1

MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
type: SiteQuality
SIO_000300: 1.508462e6

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 392
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 424
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 29437
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 197
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1226
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5747
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1003
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 50427
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66202
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.136e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.86e-1

DP
type: SiteQuality
SIO_000300: 1.509948e6

VQSLOD
type: SiteQuality
SIO_000300: 4.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.16e-1

FS
type: SiteQuality
SIO_000300: 4.669e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.87e-1

GenotypeDepth
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 145
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29437
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23699
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 424
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5589
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 665
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5747
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1003
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1226
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50427
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.042113531313253e-5
allele num: 66202
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.669e0

MQRankSum
type: SiteQuality
SIO_000300: -2.87e-1

DP
type: SiteQuality
SIO_000300: 1.509948e6

QD
type: SiteQuality
SIO_000300: 1.136e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.86e-1

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 101
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 346
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 189
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 275
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50811
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1231
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 994
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5769
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507658907248824e-5
allele num: 66328
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10188
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.581e0

VQSLOD
type: SiteQuality
SIO_000300: 6.68e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.12e-1

QD
type: SiteQuality
SIO_000300: 1.013e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.503e0

DP
type: SiteQuality
SIO_000300: 1.513167e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.363e0

GenotypeDepth
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24039
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 243
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 664
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5603
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 189
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 51013
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5778
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1227
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66442
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

MQ
type: SiteQuality
SIO_000300: 5.718e1

QD
type: SiteQuality
SIO_000300: 1.306e1

VQSLOD
type: SiteQuality
SIO_000300: -2.255e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.257e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 4.966e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.399e0

DP
type: SiteQuality
SIO_000300: 1.516922e6

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29566
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 668
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5617
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 63
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 8
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5787
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51218
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1226
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 998
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.013771536819316e-5
allele num: 66514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.48e-1

DP
type: SiteQuality
SIO_000300: 1.519566e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.367e0

FS
type: SiteQuality
SIO_000300: 1.493e0

VQSLOD
type: SiteQuality
SIO_000300: 2.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

QD
type: SiteQuality
SIO_000300: 1.022e1

MQ
type: SiteQuality
SIO_000300: 5.916e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-2

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 187
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24278
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 75
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 51272
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 997
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5791
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1230
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66600
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.697439875872769e-5
allele num: 10312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.096e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-2

QD
type: SiteQuality
SIO_000300: 1.435e1

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.52178e6

VQSLOD
type: SiteQuality
SIO_000300: 9.95e-1

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29604
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5645
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 184
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24355
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5806
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51515
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.438e1

VQSLOD
type: SiteQuality
SIO_000300: -2.107e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.16e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.368e0

MQRankSum
type: SiteQuality
SIO_000300: 3.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.74e-1

DP
type: SiteQuality
SIO_000300: 1.523882e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.54e-1

GenotypeDepth
all individuals: 185
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24367
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 668
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5644
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5802
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1228
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51550
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 9.75e1
variant carriers: 2

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999400119976005e-5
allele num: 66680
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.524178e6

VQSLOD
type: SiteQuality
SIO_000300: 9.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 3.169e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.396e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.507e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.98e-1

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 9
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24382
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 669
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 29599
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 185
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51565
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 144
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1230
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5809
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 993
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999040307101727e-5
allele num: 66688
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: 9.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.486e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.83e0

DP
type: SiteQuality
SIO_000300: 1.524418e6

QD
type: SiteQuality
SIO_000300: 1.302e1

FS
type: SiteQuality
SIO_000300: 5.999e0

VQSLOD
type: SiteQuality
SIO_000300: 7.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

GenotypeDepth
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 29598
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5646
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 994
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51577
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5811
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.011e0

VQSLOD
type: SiteQuality
SIO_000300: -3.059e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.943e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.371e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.421e0

QD
type: SiteQuality
SIO_000300: 1.306e1

DP
type: SiteQuality
SIO_000300: 1.524403e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

GenotypeDepth
all individuals: 24392
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29602
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5645
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 184
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51586
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 429
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1230
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5813
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 992
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.368000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.071e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 7.18e-1

FS
type: SiteQuality
SIO_000300: 4.465e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

QD
type: SiteQuality
SIO_000300: 1.439e1

DP
type: SiteQuality
SIO_000300: 1.524484e6

GenotypeDepth
all individuals: 5651
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 670
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29608
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 184
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24407
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 51617
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1233
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5813
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495863805299125e-5
allele num: 66728
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

DP
type: SiteQuality
SIO_000300: 1.525193e6

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

FS
type: SiteQuality
SIO_000300: 5.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.18e0

QD
type: SiteQuality
SIO_000300: 1.305e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.073e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.764e0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24413
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5654
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 670
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 2

GenotypeDepth
all individuals: 7
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 142
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 51621
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1230
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5812
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.397722163944253e-4
allele num: 66730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

DP
type: SiteQuality
SIO_000300: 1.526239e6

QD
type: SiteQuality
SIO_000300: 1.217e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 670
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 186
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 156
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51650
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1230
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5811
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.294e1

MQRankSum
type: SiteQuality
SIO_000300: 6.58e-1

FS
type: SiteQuality
SIO_000300: 1.1397e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.941e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.99e-1

DP
type: SiteQuality
SIO_000300: 1.525149e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.68e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.467e0

GenotypeDepth
all individuals: 24437
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 670
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5657
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 183
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29599
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51656
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1230
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5810
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.806e0

MQRankSum
type: SiteQuality
SIO_000300: -9.28e-1

QD
type: SiteQuality
SIO_000300: 1.787e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.836e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.67e0

VQSLOD
type: SiteQuality
SIO_000300: -1.653e0

DP
type: SiteQuality
SIO_000300: 1.525352e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

GenotypeDepth
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 667
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29595
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 184
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 9.75e1
variant carriers: 11

GenotypeDepth
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 5808
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51659
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1230
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 13
allele frequency: 1.122819139747797e-3
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.212e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.73e-1

QD
type: SiteQuality
SIO_000300: 1.461e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.649999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.6e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

DP
type: SiteQuality
SIO_000300: 1.526482e6

VQSLOD
type: SiteQuality
SIO_000300: 7.34e-1

GenotypeDepth
all individuals: 5658
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29583
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 184
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24447
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 994
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51659
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1231
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5811
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

DP
type: SiteQuality
SIO_000300: 1.525354e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

FS
type: SiteQuality
SIO_000300: 1.1303e1

VQSLOD
type: SiteQuality
SIO_000300: -1.356e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-2

QD
type: SiteQuality
SIO_000300: 1.314e1

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 183
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 671
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29576
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 24443
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51649
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 992
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5815
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.14e-1

QD
type: SiteQuality
SIO_000300: 1.511e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.01e-1

FS
type: SiteQuality
SIO_000300: 1.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.879999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.525404e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

GenotypeDepth
all individuals: 29569
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5666
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 670
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 993
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5815
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1227
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51646
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.593e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.971e1

MQRankSum
type: SiteQuality
SIO_000300: 2.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

DP
type: SiteQuality
SIO_000300: 1.525483e6

FS
type: SiteQuality
SIO_000300: 5.789e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.033e0

QD
type: SiteQuality
SIO_000300: 1.32e1

GenotypeDepth
all individuals: 670
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5663
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 185
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29569
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 24445
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51651
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1227
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5814
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 992
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495459585818323e-5
allele num: 66734
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.326e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.44e-1

DP
type: SiteQuality
SIO_000300: 1.525608e6

QD
type: SiteQuality
SIO_000300: 5.77e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.985e1

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29539
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24459
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 669
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51627
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5820
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.03e-1

DP
type: SiteQuality
SIO_000300: 1.525539e6

MQ
type: SiteQuality
SIO_000300: 5.977e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.456e0

FS
type: SiteQuality
SIO_000300: 2.866e0

MQRankSum
type: SiteQuality
SIO_000300: 8.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

VQSLOD
type: SiteQuality
SIO_000300: 9.75e-1

QD
type: SiteQuality
SIO_000300: 1.409e1

GenotypeDepth
all individuals: 24468
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 29533
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 671
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5823
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51626
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.523e0

DP
type: SiteQuality
SIO_000300: 1.5254e6

VQSLOD
type: SiteQuality
SIO_000300: -1.853e0

QD
type: SiteQuality
SIO_000300: 2.083e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.296e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.23e0

GenotypeDepth
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 183
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5672
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29533
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1224
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5822
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51627
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.541e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

DP
type: SiteQuality
SIO_000300: 1.525396e6

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

QD
type: SiteQuality
SIO_000300: 2.139e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.426e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.239e0

GenotypeDepth
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5673
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5821
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 990
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 51623
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.517e0

MQRankSum
type: SiteQuality
SIO_000300: -1.143e0

VQSLOD
type: SiteQuality
SIO_000300: 1.89e-1

DP
type: SiteQuality
SIO_000300: 1.525478e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.24e-1

FS
type: SiteQuality
SIO_000300: 2.198e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.307e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.51e-1

GenotypeDepth
all individuals: 669
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 29524
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24478
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5814
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51633
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.278e0

MQRankSum
type: SiteQuality
SIO_000300: -2.079e0

QD
type: SiteQuality
SIO_000300: 1.274e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.91e-1

FS
type: SiteQuality
SIO_000300: 5.779e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.323e0

DP
type: SiteQuality
SIO_000300: 1.525581e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-2

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5670
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29522
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5815
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1220
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51629
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

DP
type: SiteQuality
SIO_000300: 1.52577e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.409999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.1e-1

QD
type: SiteQuality
SIO_000300: 1.175e1

FS
type: SiteQuality
SIO_000300: 1.822e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.89e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeDepth
all individuals: 180
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24482
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5673
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5817
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 983
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51655
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.454828122300915e-4
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.941e1

VQSLOD
type: SiteQuality
SIO_000300: 5.580000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.429e0

QD
type: SiteQuality
SIO_000300: 1.26e1

FS
type: SiteQuality
SIO_000300: 1.779e0

DP
type: SiteQuality
SIO_000300: 1.525866e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e0

GenotypeDepth
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5678
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24491
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 182
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29526
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5824
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 984
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51675
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 135
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.93e-1

DP
type: SiteQuality
SIO_000300: 1.5258e6

MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

VQSLOD
type: SiteQuality
SIO_000300: 8.06e-1

FS
type: SiteQuality
SIO_000300: 5.153e0

QD
type: SiteQuality
SIO_000300: 1.46e1

GenotypeDepth
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5677
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 182
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29524
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 668
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51675
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 984
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5825
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.84e0

VQSLOD
type: SiteQuality
SIO_000300: 3.56e-1

DP
type: SiteQuality
SIO_000300: 1.525789e6

FS
type: SiteQuality
SIO_000300: 6.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.227e0

QD
type: SiteQuality
SIO_000300: 1.253e1

MQ
type: SiteQuality
SIO_000300: 5.984e1

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24502
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29514
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 667
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5677
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1224
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51682
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 424
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 983
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5821
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.525833e6

FS
type: SiteQuality
SIO_000300: 9.881e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.98e-1

QD
type: SiteQuality
SIO_000300: 1.388e1

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: -7.879e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.041e0

GenotypeDepth
all individuals: 24497
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 668
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.75e1
variant carriers: 25

GenotypeQuality
all individuals: 51668
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 982
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5818
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 25
allele frequency: 2.159267576438072e-3
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.35e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.05e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.1e-2

QD
type: SiteQuality
SIO_000300: 1.273e1

DP
type: SiteQuality
SIO_000300: 1.530166e6

GenotypeDepth
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5680
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24512
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 182
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 670
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29500
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 983
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5818
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51693
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.082e0

QD
type: SiteQuality
SIO_000300: 1.235e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.16e-1