http://identifiers.org/exac.variant/8-33310950-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33310950
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33310950
    reference: chr 8
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.160G>T
  hgvsp: ENSP00000332757.5:p.Glu54Ter
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-65G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.504G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.483G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.521G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.76G>T
  hgvsp: ENSP00000430428.1:p.Glu26Ter
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.142G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.76G>T
  hgvsp: ENSP00000429870.1:p.Glu26Ter
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.131G>T
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37709
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5335
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2504
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu54Ter
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/8-33310951-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33310951
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33310951
    reference: chr 8
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.159G>T
  hgvsp: ENSP00000332757.5:p.Glu53Asp
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.141G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.130G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.503G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-66G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.482G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.520G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.75G>T
  hgvsp: ENSP00000429870.1:p.Glu25Asp
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.75G>T
  hgvsp: ENSP00000430428.1:p.Glu25Asp
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2502
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu53Asp
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ

8-33310959-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33310959
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33310959
    reference: chr 8
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.133A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.151A>G
  hgvsp: ENSP00000332757.5:p.Lys51Glu
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.474A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.512A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.67A>G
  hgvsp: ENSP00000429870.1:p.Lys23Glu
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-74A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.67A>G
  hgvsp: ENSP00000430428.1:p.Lys23Glu
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.122A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.495A>G
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 965
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6677
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5125
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Lys51Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

8-33310959-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33310959
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33310959
    reference: chr 8
allele count: 5
allele frequency: 4.124187535055594e-5
allele num: 121236
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.122A>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.133A>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.67A>C
  hgvsp: ENSP00000430428.1:p.Lys23Gln
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.495A>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-74A>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.67A>C
  hgvsp: ENSP00000429870.1:p.Lys23Gln
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.151A>C
  hgvsp: ENSP00000332757.5:p.Lys51Gln
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.512A>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.474A>C
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3190
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys51Gln
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD

8-33310960-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33310960
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33310960
    reference: chr 8
allele count: 54
allele frequency: 4.455224988861938e-4
allele num: 121206
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.121A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.132A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.66A>G
  hgvsp: ENST00000518672.1:c.66A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.150A>G
  hgvsp: ENST00000327671.5:c.150A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.494A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.511A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.66A>G
  hgvsp: ENST00000524021.1:c.66A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-75A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.473A>G
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38369
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2499
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr50Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

8-33310963-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33310963
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33310963
    reference: chr 8
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.147T>C
  hgvsp: ENST00000327671.5:c.147T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.118T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.491T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.63T>C
  hgvsp: ENST00000518672.1:c.63T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.508T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.470T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.129T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-78T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.63T>C
  hgvsp: ENST00000524021.1:c.63T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3184
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6662
  bin: 6.75e1
  variant carriers: 0
hgvs: p.His49His
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

8-33310968-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33310968
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33310968
    reference: chr 8
allele count: 2
allele frequency: 1.653138483410755e-5
allele num: 120982
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.142G>A
  hgvsp: ENSP00000332757.5:p.Gly48Arg
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.124G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.465G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.58G>A
  hgvsp: ENSP00000429870.1:p.Gly20Arg
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-83G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.503G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.58G>A
  hgvsp: ENSP00000430428.1:p.Gly20Arg
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.113G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.486G>A
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10737
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2327
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly48Arg
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

8-33310969-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33310969
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33310969
    reference: chr 8
allele count: 1
allele frequency: 8.267879288962381e-6
allele num: 120950
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-84T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.57T>C
  hgvsp: ENST00000518672.1:c.57T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.123T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.502T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.485T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.112T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.57T>C
  hgvsp: ENST00000524021.1:c.57T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.141T>C
  hgvsp: ENST00000327671.5:c.141T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.464T>C
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38101
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp47Asp
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

8-33310989-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33310989
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33310988
    reference: chr 8
allele count: 2
allele frequency: 1.672436572842975e-5
allele num: 119586
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.443delT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.481delT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.120delT
  hgvsp: ENSP00000332757.5:p.Phe40LeufsTer29
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.36delT
  hgvsp: ENSP00000430428.1:p.Phe12LeufsTer29
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.91delT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.36delT
  hgvsp: ENSP00000429870.1:p.Phe12LeufsTer29
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.102delT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.464delT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-105delT
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1637
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2472
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Phe40LeufsTer29
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: TA
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/8-33311011-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33311011
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33311011
    reference: chr 8
allele count: 1
allele frequency: 8.554466286848364e-6
allele num: 116898
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.70G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.443G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.99G>T
  hgvsp: ENST00000327671.5:c.99G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.422G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.15G>T
  hgvsp: ENST00000518672.1:c.15G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.15G>T
  hgvsp: ENST00000524021.1:c.15G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-126G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.460G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.81G>T
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2451
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34241
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly33Gly
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/8-33311012-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33311012
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33311012
    reference: chr 8
allele count: 1
allele frequency: 8.570008398608231e-6
allele num: 116686
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.14G>T
  hgvsp: ENSP00000430428.1:p.Gly5Val
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.14G>T
  hgvsp: ENSP00000429870.1:p.Gly5Val
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.98G>T
  hgvsp: ENSP00000332757.5:p.Gly33Val
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.459G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.80G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.442G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.69G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.421G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-127G>T
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34326
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34049
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly33Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/8-33311017-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33311017
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33311017
    reference: chr 8
allele count: 7
allele frequency: 6.028038992800799e-5
allele num: 116124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.454G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.64G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.9G>T
  hgvsp: ENSP00000430428.1:p.Glu3Asp
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.9G>T
  hgvsp: ENSP00000429870.1:p.Glu3Asp
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.437G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-132G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.75G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.416G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.93G>T
  hgvsp: ENSP00000332757.5:p.Glu31Asp
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3877
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu31Asp
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD

8-33311017-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33311017
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33311017
    reference: chr 8
allele count: 1
allele frequency: 8.611484275429714e-6
allele num: 116124
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.437G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.64G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.416G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.9G>A
  hgvsp: ENST00000518672.1:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.454G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-132G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.93G>A
  hgvsp: ENST00000327671.5:c.93G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.75G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.9G>A
  hgvsp: ENST00000524021.1:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2449
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33917
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3153
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu31Glu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: C
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/8-33311022-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33311022
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33311022
    reference: chr 8
allele count: 1
allele frequency: 8.653663095588363e-6
allele num: 115558
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.449G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.432G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.411G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-137G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.88G>T
  hgvsp: ENSP00000332757.5:p.Val30Phe
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.4G>T
  hgvsp: ENSP00000429870.1:p.Val2Phe
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.4G>T
  hgvsp: ENSP00000430428.1:p.Val2Phe
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.59G>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.70G>T
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4010
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2447
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val30Phe
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

8-33311027-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33311027
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33311027
    reference: chr 8
allele count: 2
allele frequency: 1.739765827519616e-5
allele num: 114958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-2T>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-2T>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.54T>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-142T>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.444T>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.406T>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.83T>A
  hgvsp: ENSP00000332757.5:p.Val28Asp
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.65T>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.427T>A
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3968
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val28Asp
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

8-33311034-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33311034
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33311034
    reference: chr 8
allele count: 1
allele frequency: 8.785647765809773e-6
allele num: 113822
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-6T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-6T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-6T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-6T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.64-6T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-6T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-6T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-6T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.53-6T>C
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3661
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
hgvs: c.82-6T>C
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

8-33311035-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33311035
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33311035
    reference: chr 8
allele count: 1
allele frequency: 8.785184664581649e-6
allele num: 113828
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-7C>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-7C>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-7C>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-7C>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-7C>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-7C>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-7C>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.53-7C>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.64-7C>G
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6300
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3697
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
hgvs: c.82-7C>G
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-33311035-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33311035
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33311035
    reference: chr 8
allele count: 2
allele frequency: 1.75703693291633e-5
allele num: 113828
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-7C>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-7C>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-7C>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-7C>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-7C>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.53-7C>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-7C>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.64-7C>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-7C>A
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 2.75e1
  variant carriers: 0
hgvs: c.82-7C>A
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

8-33311050-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33311050
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33311050
    reference: chr 8
allele count: 1
allele frequency: 8.926339843610525e-6
allele num: 112028
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-22T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-22T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.64-22T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-22T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-22T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.53-22T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-22T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-22T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-22T>C
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5075
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1232
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2319
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2314
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

8-33311064-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33311064
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33311064
    reference: chr 8
allele count: 2
allele frequency: 1.802223944347325e-5
allele num: 110974
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-36C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-36C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-36C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-36C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-36C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.64-36C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.53-36C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-36C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-36C>T
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9107
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6243
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5176
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1594
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

8-33311079-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33311079
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33311079
    reference: chr 8
allele count: 1
allele frequency: 9.064539521392313e-6
allele num: 110320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-51C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-51C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-51C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-51C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.53-51C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-51C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-51C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-51C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.64-51C>T
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2418
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3136
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5174
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31414
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-33313240-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313240
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313240
    reference: chr 8
allele count: 2
allele frequency: 1.40016802016242e-4
allele num: 14284
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2212A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2212A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.63+48A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2212A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.52+48A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2212A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2212A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2212A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2212A>G
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1898
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

8-33313245-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313245
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313245
    reference: chr 8
allele count: 5
allele frequency: 3.497971176717504e-4
allele num: 14294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.63+43A>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2217A>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2217A>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2217A>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2217A>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2217A>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2217A>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.52+43A>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2217A>C
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

8-33313263-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313263
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313263
    reference: chr 8
allele count: 247
allele frequency: 1.724137931034483e-2
allele num: 14326
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2235G>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2235G>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.52+25G>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2235G>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2235G>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.63+25G>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2235G>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2235G>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2235G>C
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 3.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 2.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.5e0
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 3.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 2.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 2.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1857
  bin: 7.5e0
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 2.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 7.25e1
  variant carriers: 3
num of homozygotes: 7
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

8-33313300-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313300
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313300
    reference: chr 8
allele count: 2
allele frequency: 1.376651982378855e-4
allele num: 14528
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2272G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.40G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2272G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.51G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2272G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2272G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2272G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2272G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2272G>A
  variant of: http://identifiers.org/hgnc/19234
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2920
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-33313302-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313302
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313302
    reference: chr 8
allele count: 1
allele frequency: 6.88041832943443e-5
allele num: 14534
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.38G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2274G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2274G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2274G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2274G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2274G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2274G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.49G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2274G>A
  variant of: http://identifiers.org/hgnc/19234
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2947
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1889
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD

8-33313321-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313321
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313321
    reference: chr 8
allele count: 7
allele frequency: 4.795177421564598e-4
allele num: 14598
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.30A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2293A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2293A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2293A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2293A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2293A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.19A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2293A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2293A>G
  variant of: http://identifiers.org/hgnc/19234
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 9.75e1
  variant carriers: 7
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

8-33313328-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313328
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313328
    reference: chr 8
allele count: 1
allele frequency: 6.84369011771147e-5
allele num: 14612
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2300G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2300G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2300G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2300G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.23G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2300G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.12G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2300G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2300G>A
  variant of: http://identifiers.org/hgnc/19234
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

8-33313329-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313329
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313329
    reference: chr 8
allele count: 8647
allele frequency: 5.840199918951776e-1
allele num: 14806
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2301C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.22C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2301C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.11C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2301C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2301C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2301C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2301C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2301C>T
  variant of: http://identifiers.org/hgnc/19234
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.25e1
  variant carriers: 466
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.5e0
  variant carriers: 536
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 389
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 2.75e1
  variant carriers: 177
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 229
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.25e1
  variant carriers: 137
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 5.75e1
  variant carriers: 336
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 2.5e0
  variant carriers: 425
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 3.25e1
  variant carriers: 166
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 7.75e1
  variant carriers: 442
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 9.75e1
  variant carriers: 1297
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 326
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.75e1
  variant carriers: 440
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 3.75e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.25e1
  variant carriers: 201
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.25e1
  variant carriers: 438
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 375
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 192
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 2.25e1
  variant carriers: 185
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 7.25e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 37
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 9.25e1
  variant carriers: 48
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 7.75e1
  variant carriers: 42
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.25e1
  variant carriers: 62
num of homozygotes: 2596
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

8-33313337-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313337
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313337
    reference: chr 8
allele count: 5
allele frequency: 3.453515678961182e-4
allele num: 14478
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2309A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2309A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2309A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2309A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000518076
  gene symbol: FUT10
  hgvsc: ENST00000518076.1:n.3A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2309A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520935
  gene symbol: FUT10
  hgvsc: ENST00000520935.1:n.14A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2309A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2309A>G
  variant of: http://identifiers.org/hgnc/19234
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3788
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

8-33313371-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313371
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313371
    reference: chr 8
allele count: 1
allele frequency: 7.047216349541931e-5
allele num: 14190
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2343C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2343C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2343C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2343C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2343C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2343C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2343C>T
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3647
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

8-33313378-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313378
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313378
    reference: chr 8
allele count: 1
allele frequency: 7.051191651389085e-5
allele num: 14182
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2350G>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2350G>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2350G>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2350G>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2350G>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2350G>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2350G>C
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1779
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

8-33313378-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313378
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313378
    reference: chr 8
allele count: 1
allele frequency: 7.051191651389085e-5
allele num: 14182
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2350G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2350G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2350G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2350G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2350G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2350G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2350G>A
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3590
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

8-33313389-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313389
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313389
    reference: chr 8
allele count: 1
allele frequency: 7.068136839129205e-5
allele num: 14148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2361A>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2361A>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2361A>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2361A>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2361A>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2361A>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2361A>T
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3434
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1661
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1496
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

8-33313401-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313401
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313401
    reference: chr 8
allele count: 1
allele frequency: 7.122507122507122e-5
allele num: 14040
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2373G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2373G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2373G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2373G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2373G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2373G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2373G>A
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3070
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/8-33313414-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313414
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313415
    reference: chr 8
allele count: 290
allele frequency: 2.651307368805998e-2
allele num: 10938
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2387dupT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2387dupT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2387dupT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2387dupT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2387dupT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2387dupT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2387dupT
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 2.75e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 3.25e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 4.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 3.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 2.25e1
  variant carriers: 54
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 7.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 8.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 2.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 9.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 1074
  bin: 7.5e0
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 5.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 2.5e0
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 2.75e1
  variant carriers: 13
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-33313414-C-CAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313414
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313416
    reference: chr 8
allele count: 38
allele frequency: 3.474126897056135e-3
allele num: 10938
alternate allele: CAA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2388_443-2387dupTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2388_-3-2387dupTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2388_-143-2387dupTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2388_82-2387dupTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2388_426-2387dupTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2388_-3-2387dupTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2388_405-2387dupTT
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 2.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1074
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 9.75e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 2.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 2.75e1
  variant carriers: 2
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/8-33313414-C-CAAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313414
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313417
    reference: chr 8
allele count: 1
allele frequency: 9.142439202779301e-5
allele num: 10938
alternate allele: CAAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2389_-3-2387dupTTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2389_443-2387dupTTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2389_82-2387dupTTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2389_426-2387dupTTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2389_-143-2387dupTTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2389_405-2387dupTTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2389_-3-2387dupTTT
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1074
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-33313419-AAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313419
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313417
    reference: chr 8
allele count: 2
allele frequency: 1.615769914364195e-4
allele num: 12378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2393_-3-2392delCT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2393_82-2392delCT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2393_443-2392delCT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2393_405-2392delCT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2393_426-2392delCT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2393_-143-2392delCT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2393_-3-2392delCT
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1038
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1231
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: AAG
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ

8-33313420-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313420
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313419
    reference: chr 8
allele count: 213
allele frequency: 2.076023391812866e-2
allele num: 10260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2393delC
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2393delC
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2393delC
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2393delC
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2393delC
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2393delC
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2393delC
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 2.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 3.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 2.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 4.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 3.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 8.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 5.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 9.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 2.5e0
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 9.75e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 7.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 6.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 4.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 7.5e0
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 3.75e1
  variant carriers: 18
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
reference allele: AG
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

8-33313421-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313421
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313420
    reference: chr 8
allele count: 4014
allele frequency: 3.812689969604863e-1
allele num: 10528
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2394delT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2394delT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2394delT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2394delT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2394delT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2394delT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2394delT
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 3.25e1
  variant carriers: 653
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 372
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.25e1
  variant carriers: 210
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 2.75e1
  variant carriers: 883
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 1.75e1
  variant carriers: 716
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 141
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.5e0
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 405
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 138
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 2.25e1
  variant carriers: 944
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.75e1
  variant carriers: 170
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 7.75e1
  variant carriers: 144
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 7.5e0
  variant carriers: 228
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 4.75e1
  variant carriers: 180
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 2.25e1
  variant carriers: 180
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 7.25e1
  variant carriers: 149
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 4.25e1
  variant carriers: 161
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 6.75e1
  variant carriers: 132
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 3.25e1
  variant carriers: 184
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 1.25e1
  variant carriers: 192
num of homozygotes: 149
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: GA
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-33313421-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313421
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313421
    reference: chr 8
allele count: 1708
allele frequency: 1.622340425531915e-1
allele num: 10528
alternate allele: A
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 1.75e1
  variant carriers: 127
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 2.25e1
  variant carriers: 272
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 3.25e1
  variant carriers: 392
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.25e1
  variant carriers: 209
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 333
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 2.75e1
  variant carriers: 401
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 41
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 9.25e1
  variant carriers: 43
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 3.25e1
  variant carriers: 66
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 4.75e1
  variant carriers: 57
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 8.25e1
  variant carriers: 52
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.75e1
  variant carriers: 58
genotype quality: GenotypeQuality
  all individuals: 2430
  bin: 9.75e1
  variant carriers: 882
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 7.5e0
  variant carriers: 68
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 1.25e1
  variant carriers: 59
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 6.75e1
  variant carriers: 55
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 5.75e1
  variant carriers: 57
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 5.25e1
  variant carriers: 47
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 2.5e0
  variant carriers: 69
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 2.25e1
  variant carriers: 65
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 8.75e1
  variant carriers: 51
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 7.75e1
  variant carriers: 56
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 4.25e1
  variant carriers: 60
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 1.75e1
  variant carriers: 67
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 7.25e1
  variant carriers: 57
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 6.25e1
  variant carriers: 58
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 2.75e1
  variant carriers: 51
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1174
  allele frequency: 2.040319777546055e-1
  allele num: 5754
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 80
  allele frequency: 5.805515239477504e-2
  allele num: 1378
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 365
  allele frequency: 1.366017964071856e-1
  allele num: 2672
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 19
  allele frequency: 1.696428571428572e-1
  allele num: 112
  num of homozygotes: 0
population: African
population: Other
population: East Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

8-33313421-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313421
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313422
    reference: chr 8
allele count: 272
allele frequency: 2.583586626139818e-2
allele num: 10528
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2394dupT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2394dupT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2394dupT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2394dupT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2394dupT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2394dupT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2394dupT
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 1.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 2.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 2.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 3.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 6.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 1.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 8.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 2.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 3.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 4.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 5.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2430
  bin: 9.75e1
  variant carriers: 124
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 8.75e1
  variant carriers: 8
num of homozygotes: 2
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

8-33313421-G-GAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313421
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313423
    reference: chr 8
allele count: 2
allele frequency: 1.899696048632219e-4
allele num: 10528
alternate allele: GAA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2395_426-2394dupTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2395_405-2394dupTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2395_82-2394dupTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2395_-3-2394dupTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2395_443-2394dupTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2395_-143-2394dupTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2395_-3-2394dupTT
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

8-33313421-GAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313421
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313419
    reference: chr 8
allele count: 98
allele frequency: 9.308510638297872e-3
allele num: 10528
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2395_-3-2394delTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2395_82-2394delTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2395_-3-2394delTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2395_443-2394delTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2395_426-2394delTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2395_405-2394delTT
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2395_-143-2394delTT
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 2.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 2.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 1.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2430
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 1.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 5.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 1.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 2.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 4.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 2.5e0
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 4.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 7.5e0
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.75e1
  variant carriers: 12
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: GAA
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

8-33313421-GAAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313421
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313418
    reference: chr 8
allele count: 1
allele frequency: 9.498480243161094e-5
allele num: 10528
alternate allele: G
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2430
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1378
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 3.74251497005988e-4
  allele num: 2672
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 142
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 112
  num of homozygotes: 0
population: East Asian
population: South Asian
population: African
reference allele: GAAA
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

8-33313435-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33313435
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33313435
    reference: chr 8
allele count: 1
allele frequency: 7.836990595611286e-5
allele num: 12760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.426-2407T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.82-2407T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.443-2407T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-143-2407T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.405-2407T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-3-2407T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-3-2407T>C
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1021
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1214
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

8-33318856-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318856
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318856
    reference: chr 8
allele count: 1
allele frequency: 8.833610119783754e-6
allele num: 113204
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+150C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.425+34C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-4+74C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-144+34C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.81+34C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.382+34C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.404+34C>T
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7446
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-33318859-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318859
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318859
    reference: chr 8
allele count: 6
allele frequency: 5.293899662955055e-5
allele num: 113338
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.425+31T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.81+31T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.404+31T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.382+31T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-4+71T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+147T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-144+31T>C
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11280
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12427
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28453
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1149
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum

8-33318860-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318860
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318860
    reference: chr 8
allele count: 13
allele frequency: 1.146971113973637e-4
allele num: 113342
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-4+70A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+146A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.382+30A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-144+30A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.425+30A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.404+30A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.81+30A>G
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12460
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11291
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3052
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42862
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1380
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

8-33318862-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318862
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318862
    reference: chr 8
allele count: 1
allele frequency: 8.813834194151139e-6
allele num: 113458
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.382+28T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.404+28T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.81+28T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+144T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-4+68T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.425+28T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-144+28T>C
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1376
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3009
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 890
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

8-33318880-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318880
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318880
    reference: chr 8
allele count: 1
allele frequency: 8.70716076901644e-6
allele num: 114848
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.382+10A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.425+10A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.81+10A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-4+50A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.404+10A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+126A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-144+10A>G
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1388
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 890
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

8-33318890-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318890
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318890
    reference: chr 8
allele count: 13
allele frequency: 1.123051936832648e-4
allele num: 115756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.425G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.404G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.382G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+116G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-144G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.81G>A
  hgvsp: ENST00000327671.5:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-4+40G>A
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13511
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7543
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2705
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44124
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
hgvs: c.81G>A
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

8-33318891-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318891
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318891
    reference: chr 8
allele count: 402
allele frequency: 3.46689204339652e-3
allele num: 115954
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-4+39A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-145A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.381A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.80A>G
  hgvsp: ENSP00000332757.5:p.Gln27Arg
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.424A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.403A>G
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+115A>G
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.75e1
  variant carriers: 123
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11297
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 28740
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13581
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.25e1
  variant carriers: 1
hgvs: p.Gln27Arg
num of homozygotes: 2
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum

8-33318892-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318892
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318892
    reference: chr 8
allele count: 2
allele frequency: 1.722534192303717e-5
allele num: 116108
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.380C>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-4+38C>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+114C>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.79C>A
  hgvsp: ENSP00000332757.5:p.Gln27Lys
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.402C>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-146C>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.423C>A
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28962
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44593
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2609
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7592
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gln27Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum

8-33318895-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318895
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318895
    reference: chr 8
allele count: 1
allele frequency: 8.589589417625837e-6
allele num: 116420
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.76C>A
  hgvsp: ENSP00000332757.5:p.Leu26Ile
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+111C>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-4+35C>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-149C>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.377C>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.420C>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.399C>A
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29003
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7602
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1133
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu26Ile
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

8-33318911-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318911
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318911
    reference: chr 8
allele count: 3
allele frequency: 2.531389226407453e-5
allele num: 118512
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-165C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+95C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.404C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.361C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.60C>T
  hgvsp: ENST00000327671.5:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.383C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-4+19C>T
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15173
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1521
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7699
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val20Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-33318913-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318913
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318913
    reference: chr 8
allele count: 1228
allele frequency: 1.033774455332188e-2
allele num: 118788
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.381G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+93G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.402G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-4+17G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-167G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.58G>A
  hgvsp: ENSP00000332757.5:p.Val20Ile
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.359G>A
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 3.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 1.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 15107
  bin: 2.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.75e1
  variant carriers: 308
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 11258
  bin: 3.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 29309
  bin: 2.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 60
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1323
  bin: 9.75e1
  variant carriers: 1209
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7606
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 7.25e1
  variant carriers: 1
hgvs: p.Val20Ile
num of homozygotes: 16
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ

8-33318914-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318914
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318914
    reference: chr 8
allele count: 9
allele frequency: 7.553884375209831e-5
allele num: 119144
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.380C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.57C>T
  hgvsp: ENST00000327671.5:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-168C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-4+16C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.401C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.358C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+92C>T
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1217
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr19Thr
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

8-33318923-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318923
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318923
    reference: chr 8
allele count: 1
allele frequency: 8.320713584396998e-6
allele num: 120182
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.392C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.48C>T
  hgvsp: ENST00000327671.5:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-4+7C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.371C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-177C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+83C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.349C>T
  variant of: http://identifiers.org/hgnc/19234
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11531
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7914
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1401
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48131
  bin: 6.25e1
  variant carriers: 0
hgvs: c.-4+7C>T
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

8-33318925-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318925
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318925
    reference: chr 8
allele count: 5
allele frequency: 4.157450983652902e-5
allele num: 120266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-4+5G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.390G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-179G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.369G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+81G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.46G>A
  hgvsp: ENSP00000332757.5:p.Val16Ile
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.347G>A
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7904
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1403
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1109
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48136
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val16Ile
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

8-33318926-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318926
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318926
    reference: chr 8
allele count: 13
allele frequency: 1.079536961684742e-4
allele num: 120422
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.45C>T
  hgvsp: ENST00000327671.5:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-4+4C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.368C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.346C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+80C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-180C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.389C>T
  variant of: http://identifiers.org/hgnc/19234
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30315
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1109
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
hgvs: c.-4+4C>T
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

8-33318929-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318929
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318929
    reference: chr 8
allele count: 1
allele frequency: 8.290224167661493e-6
allele num: 120624
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.386G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-4+1G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-183G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.343G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+77G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.42G>A
  hgvsp: ENST00000327671.5:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.365G>A
  variant of: http://identifiers.org/hgnc/19234
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 48538
  bin: 6.25e1
  variant carriers: 0
hgvs: c.-4+1G>A
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

8-33318936-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318936
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318936
    reference: chr 8
allele count: 4
allele frequency: 3.308738378056447e-5
allele num: 120892
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.35C>T
  hgvsp: ENSP00000332757.5:p.Ser12Phe
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.379C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.358C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.336C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+70C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-10C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-190C>T
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48797
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser12Phe
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-33318939-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318939
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318939
    reference: chr 8
allele count: 1
allele frequency: 8.268152729317216e-6
allele num: 120946
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.333C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.376C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+67C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-13C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.32C>T
  hgvsp: ENSP00000332757.5:p.Ala11Val
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.355C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-193C>T
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1112
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48869
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala11Val
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

8-33318963-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318963
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318963
    reference: chr 8
allele count: 3
allele frequency: 2.479625741821368e-5
allele num: 120986
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.8G>A
  hgvsp: ENSP00000332757.5:p.Arg3Gln
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+43G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.331G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.352G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.309G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-217G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-37G>A
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1401
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7967
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1101
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg3Gln
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

8-33318964-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318964
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318964
    reference: chr 8
allele count: 4
allele frequency: 3.307042346677249e-5
allele num: 120954
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+42C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.351C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-38C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.330C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-218C>T
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.7C>T
  hgvsp: ENSP00000332757.5:p.Arg3Trp
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.308C>T
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7957
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48906
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg3Trp
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-33318969-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318969
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318969
    reference: chr 8
allele count: 1
allele frequency: 8.269383434771103e-6
allele num: 120928
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.303T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.2T>C
  hgvsp: ENSP00000332757.5:p.Met1?
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+37T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.325T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-43T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-223T>C
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.346T>C
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1391
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48999
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

8-33318970-T-TGCTGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318970
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318975
    reference: chr 8
allele count: 1
allele frequency: 8.27034090345204e-6
allele num: 120914
alternate allele: TGCTGC
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-229_-225dupGCAGC
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.297_301dupGCAGC
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-49_-45dupGCAGC
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.-5_-1dupGCAGC
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.319_323dupGCAGC
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.340_344dupGCAGC
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+31_-4+35dupGCAGC
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1091
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

8-33318972-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33318972
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 33318972
    reference: chr 8
allele count: 2
allele frequency: 1.654971534489607e-5
allele num: 120848
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000430428
  ensembl transcript: ENST00000518672
  gene symbol: FUT10
  hgvsc: ENST00000518672.1:c.-4+34G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000332757
  ensembl transcript: ENST00000327671
  gene symbol: FUT10
  hgvsc: ENST00000327671.5:c.-2G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520767
  gene symbol: FUT10
  hgvsc: ENST00000520767.1:n.343G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000334997
  ensembl transcript: ENST00000335589
  gene symbol: FUT10
  hgvsc: ENST00000335589.3:c.-226G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000520503
  gene symbol: FUT10
  hgvsc: ENST00000520503.1:n.300G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172728
  ensembl protein: ENSP00000429870
  ensembl transcript: ENST00000524021
  gene symbol: FUT10
  hgvsc: ENST00000524021.1:c.-46G>A
  variant of: http://identifiers.org/hgnc/19234
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172728
  ensembl transcript: ENST00000416169
  gene symbol: FUT10
  hgvsc: ENST00000416169.1:n.322G>A
  variant of: http://identifiers.org/hgnc/19234
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum

9-33442116-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33442116
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 33442116
    reference: chr 9
allele count: 1
allele frequency: 8.354637659364713e-6
allele num: 119694
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165272
  ensembl transcript: ENST00000493581
  gene symbol: AQP3
  hgvsc: ENST00000493581.1:n.1949C>T
  variant of: http://identifiers.org/hgnc/636
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165272
  ensembl transcript: ENST00000494313
  gene symbol: AQP3
  hgvsc: ENST00000494313.1:n.570C>T
  variant of: http://identifiers.org/hgnc/636
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165272
  ensembl protein: ENSP00000297991
  ensembl transcript: ENST00000297991
  gene symbol: AQP3
  hgvsc: ENST00000297991.4:c.804C>T
  hgvsp: ENST00000297991.4:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/636
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5354
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50660
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1153
  bin: 2.25e1
  variant carriers: 0
hgvs: p.His268His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G

GenotypeQuality
all individuals: 38550
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5121
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 965
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6682
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3194
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2323
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1230
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
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: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.779e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

QD
type: SiteQuality
SIO_000300: 1.164e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 9.28e-1

DP
type: SiteQuality
SIO_000300: 1.620134e6

GenotypeQuality
all individuals: 965
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38535
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6681
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5121
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3194
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2325
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 16484
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: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.03e-1

FS
type: SiteQuality
SIO_000300: 7.744e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.372e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

DP
type: SiteQuality
SIO_000300: 1.6201e6

VQSLOD
type: SiteQuality
SIO_000300: -1.494e-1

QD
type: SiteQuality
SIO_000300: 1.666e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38465
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3190
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2325
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2501
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 6.37e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.34e-1

FS
type: SiteQuality
SIO_000300: 5.46e-1

QD
type: SiteQuality
SIO_000300: 1.696e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.6e-1

DP
type: SiteQuality
SIO_000300: 1.619692e6

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
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GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.806767929244376e-4
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66650
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.619692e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.37e0

VQSLOD
type: SiteQuality
SIO_000300: 9.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 5.46e-1

QD
type: SiteQuality
SIO_000300: 1.696e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 54

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 54
allele frequency: 4.672897196261682e-3
allele num: 11556
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: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.17e-2

MQ
type: SiteQuality
SIO_000300: 5.978e1

DP
type: SiteQuality
SIO_000300: 1.623239e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.09e-1

QD
type: SiteQuality
SIO_000300: 1.509e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.15e-1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 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: 66626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16402
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.105e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.97e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 8.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.105e0

DP
type: SiteQuality
SIO_000300: 1.620013e6

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3177
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16298
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.312138728323699e-4
allele num: 8650
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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: 66560
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.88e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.547e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e0

DP
type: SiteQuality
SIO_000300: 1.617578e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.207e1

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5166
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16280
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50271992306074e-5
allele num: 66546
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: 904
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.21e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.49e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.228e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.35e-1

FS
type: SiteQuality
SIO_000300: 2.954e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.617039e6

QD
type: SiteQuality
SIO_000300: 7.6e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
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: 2
allele frequency: 3.021513173797438e-5
allele num: 66192
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.185e0

MQRankSum
type: SiteQuality
SIO_000300: -2.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQ
type: SiteQuality
SIO_000300: 6.017e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.114e0

DP
type: SiteQuality
SIO_000300: 1.596605e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52545992616774e-5
allele num: 65554
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.932e1

FS
type: SiteQuality
SIO_000300: 3.297e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

QD
type: SiteQuality
SIO_000300: 9.300000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.173e0

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 1.561007e6

VQSLOD
type: SiteQuality
SIO_000300: -3.23e-2

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
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: 11526
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65494
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.800078400627205e-5
allele num: 10204
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.02e-1

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.15e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.955e1

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.057e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 312
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 6.87757909215956e-4
allele num: 10178
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65336
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
allele num: 12996
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
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MQ
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InbreedingCoeff
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DP
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: -3.876e0

ClippingRankSum
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SIO_000300: -1.12e-1

FS
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.530549773478634e-5
allele num: 65336
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

QD
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FS
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 7.916402786573781e-5
allele num: 12632
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Other
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65188
num of homozygotes: 0

Latino
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ReadPosRankSum
type: SiteQuality
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DP
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FS
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10126
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 2
allele frequency: 1.637465203864418e-4
allele num: 12214
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65036
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.18e-1

VQSLOD
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DP
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FS
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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SIO_000300: 1.44e-1

ClippingRankSum
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SIO_000300: 1.29e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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num of homozygotes: 0

East Asian
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allele count: 1
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allele num: 8586
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

MQ
type: SiteQuality
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DP
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MQRankSum
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VQSLOD
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QD
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.52e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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ReadPosRankSum
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BaseQRankSum
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QD
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MQRankSum
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MQ
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VQSLOD
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DP
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FS
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Other
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East Asian
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South Asian
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European (Finnish)
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num of homozygotes: 0

Latino
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ReadPosRankSum
type: SiteQuality
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FS
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QD
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VQSLOD
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MQ
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BaseQRankSum
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DP
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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East Asian
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Other
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South Asian
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European (Non-Finnish)
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African
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ReadPosRankSum
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BaseQRankSum
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DP
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QD
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VQSLOD
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MQ
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FS
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558214909000249e-5
allele num: 64176
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.01010101010101e-4
allele num: 9900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.513299e6

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.684e0

QD
type: SiteQuality
SIO_000300: 1.425e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.93e-1

FS
type: SiteQuality
SIO_000300: 9.138e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.94e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: -8.0e-4

GenotypeQuality
all individuals: 1234
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63996
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9738
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.087902523933855e-4
allele num: 9192
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.12e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e-1

DP
type: SiteQuality
SIO_000300: 1.509434e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.12e-1

QD
type: SiteQuality
SIO_000300: 1.399e1

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.16e0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 246
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4006
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.668089647812167e-4
allele num: 7496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.49e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.44e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.720000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

VQSLOD
type: SiteQuality
SIO_000300: 2.28e0

DP
type: SiteQuality
SIO_000300: 1.98249e5

GenotypeQuality
all individuals: 1882
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 834
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variant carriers: 5

GenotypeQuality
all individuals: 245
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 6.600660066006601e-3
allele num: 606
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 5.263157894736842e-3
allele num: 190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4002
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1602
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.228e-1

DP
type: SiteQuality
SIO_000300: 1.99068e5

QD
type: SiteQuality
SIO_000300: 1.216e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.14e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.29e-1

FS
type: SiteQuality
SIO_000300: 3.237e0

MQRankSum
type: SiteQuality
SIO_000300: 8.75e-1

MQ
type: SiteQuality
SIO_000300: 5.855e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.07e-1

GenotypeQuality
all individuals: 432
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 500
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 222

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
all individuals: 46
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GenotypeQuality
all individuals: 350
bin: 8.25e1
variant carriers: 4

Latino
type: Population
allele count: 2
allele frequency: 1.063829787234043e-2
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 93
allele frequency: 1.529605263157895e-1
allele num: 608
num of homozygotes: 6

European (Non-Finnish)
type: Population
allele count: 59
allele frequency: 1.466202783300199e-2
allele num: 4024
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 6.25e-4
allele num: 1600
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 5.494505494505495e-3
allele num: 182
num of homozygotes: 0

South Asian
type: Population
allele count: 91
allele frequency: 1.208820403825717e-2
allele num: 7528
num of homozygotes: 1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-2

DP
type: SiteQuality
SIO_000300: 2.09428e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.573e0

MQRankSum
type: SiteQuality
SIO_000300: 2.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.98e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.09e-1

QD
type: SiteQuality
SIO_000300: 1.246e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 439
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variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.627430373095113e-4
allele num: 7612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4154
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.906e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.45e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.023e0

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

VQSLOD
type: SiteQuality
SIO_000300: -7.591e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.20659e5

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 28
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GenotypeQuality
all individuals: 189
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.313715186547556e-4
allele num: 7612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4166
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.19e-1

FS
type: SiteQuality
SIO_000300: 1.231e0

MQ
type: SiteQuality
SIO_000300: 5.874e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

VQSLOD
type: SiteQuality
SIO_000300: -2.885e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.476e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.54e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.23e-1

DP
type: SiteQuality
SIO_000300: 2.212e5

QD
type: SiteQuality
SIO_000300: 3.019e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.664289110794104e-3
allele num: 4206
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.27e-2

FS
type: SiteQuality
SIO_000300: 5.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.41e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.19e-1

QD
type: SiteQuality
SIO_000300: 1.438e1

DP
type: SiteQuality
SIO_000300: 2.22181e5

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 37
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GenotypeQuality
all individuals: 520
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.370791844476055e-4
allele num: 4218
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.070000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.22532e5

QD
type: SiteQuality
SIO_000300: 1.114e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.81e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

VQSLOD
type: SiteQuality
SIO_000300: 5.590000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.59e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 54

GenotypeQuality
all individuals: 168
bin: 1.25e1
variant carriers: 157

GenotypeQuality
all individuals: 42
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variant carriers: 41

GenotypeQuality
all individuals: 701
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variant carriers: 51

GenotypeQuality
all individuals: 649
bin: 7.5e0
variant carriers: 251

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 42

GenotypeQuality
all individuals: 216
bin: 1.75e1
variant carriers: 204

GenotypeQuality
all individuals: 307
bin: 6.75e1
variant carriers: 50

GenotypeQuality
all individuals: 5723
bin: 9.75e1
variant carriers: 5636

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 36

GenotypeQuality
all individuals: 71
bin: 8.75e1
variant carriers: 41

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 43

GenotypeQuality
all individuals: 188
bin: 2.25e1
variant carriers: 143

GenotypeQuality
all individuals: 116
bin: 8.25e1
variant carriers: 52

East Asian
type: Population
allele count: 121
allele frequency: 6.111111111111112e-1
allele num: 198
num of homozygotes: 32

European (Non-Finnish)
type: Population
allele count: 2791
allele frequency: 6.419043238270469e-1
allele num: 4348
num of homozygotes: 901

South Asian
type: Population
allele count: 3966
allele frequency: 5.206090837490155e-1
allele num: 7618
num of homozygotes: 1055

Latino
type: Population
allele count: 103
allele frequency: 5.364583333333334e-1
allele num: 192
num of homozygotes: 26

European (Finnish)
type: Population
allele count: 1031
allele frequency: 6.435705368289638e-1
allele num: 1602
num of homozygotes: 340

African
type: Population
allele count: 521
allele frequency: 7.870090634441088e-1
allele num: 662
num of homozygotes: 207

Other
type: Population
allele count: 114
allele frequency: 6.129032258064516e-1
allele num: 186
num of homozygotes: 35

MQ
type: SiteQuality
SIO_000300: 5.943e1

DP
type: SiteQuality
SIO_000300: 4.84195e5

ClippingRankSum
type: SiteQuality
SIO_000300: -4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.206e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.78e0

MQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

QD
type: SiteQuality
SIO_000300: 2.055e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.07e-1

GenotypeQuality
all individuals: 89
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1950
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 6.561679790026247e-4
allele num: 7620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4102
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1596
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.946e1

VQSLOD
type: SiteQuality
SIO_000300: -6.93e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.178e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.3e0

DP
type: SiteQuality
SIO_000300: 3.04741e5

FS
type: SiteQuality
SIO_000300: 8.26e-1

QD
type: SiteQuality
SIO_000300: 9.67e0

MQRankSum
type: SiteQuality
SIO_000300: -3.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-2

GenotypeQuality
all individuals: 1780
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1528
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312335958005249e-4
allele num: 7620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3866
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1590
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.371e1

VQSLOD
type: SiteQuality
SIO_000300: -3.692e-1

FS
type: SiteQuality
SIO_000300: 1.118e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.608e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.19e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e-1

DP
type: SiteQuality
SIO_000300: 2.98281e5

MQ
type: SiteQuality
SIO_000300: 5.909e1

GenotypeQuality
all individuals: 1515
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3590
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

DP
type: SiteQuality
SIO_000300: 2.97211e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.7e0

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.642e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.47e-2

QD
type: SiteQuality
SIO_000300: 1.019e1

GenotypeQuality
all individuals: 1779
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1515
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3860
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1590
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 550
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.642e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.47e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.97211e5

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.7e0

QD
type: SiteQuality
SIO_000300: 1.019e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

GenotypeQuality
all individuals: 64
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3838
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.9489e5

MQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

FS
type: SiteQuality
SIO_000300: 3.715e0

VQSLOD
type: SiteQuality
SIO_000300: -1.259e0

MQ
type: SiteQuality
SIO_000300: 5.767e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-1

QD
type: SiteQuality
SIO_000300: 1.242e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.77e-2

GenotypeQuality
all individuals: 139
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 407
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3762
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.314751511964239e-4
allele num: 7606
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.945e1

MQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.29e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.093e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.48e-1

MQ
type: SiteQuality
SIO_000300: 5.927e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.12e-2

DP
type: SiteQuality
SIO_000300: 2.89837e5

GenotypeQuality
all individuals: 270
bin: 1.25e1
variant carriers: 12

GenotypeQuality
all individuals: 317
bin: 1.75e1
variant carriers: 20

GenotypeQuality
all individuals: 400
bin: 9.75e1
variant carriers: 187

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 744
bin: 3.25e1
variant carriers: 10

GenotypeQuality
all individuals: 261
bin: 4.25e1
variant carriers: 7

GenotypeQuality
all individuals: 118
bin: 7.25e1
variant carriers: 9

GenotypeQuality
all individuals: 296
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 358
bin: 4.75e1
variant carriers: 5

GenotypeQuality
all individuals: 573
bin: 3.75e1
variant carriers: 10

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 4.065040650406504e-2
allele num: 246
num of homozygotes: 0

South Asian
type: Population
allele count: 189
allele frequency: 3.074170461938842e-2
allele num: 6148
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.884615384615385e-2
allele num: 104
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 3.472222222222222e-2
allele num: 144
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 73
allele frequency: 2.775665399239544e-2
allele num: 2630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 10
allele frequency: 6.631299734748011e-3
allele num: 1508
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.63419e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 3.84e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.552e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.86e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.818000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.1184e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.0e-2

GenotypeQuality
all individuals: 358
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 270
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 744
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 188
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 95
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1078
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 118
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 6.63129973474801e-4
allele num: 1508
num of homozygotes: 0

South Asian
type: Population
allele count: 19
allele frequency: 3.090435914118412e-3
allele num: 6148
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 104
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 2.032520325203252e-2
allele num: 246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 4.94296577946768e-3
allele num: 2630
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.1184e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.552e0

DP
type: SiteQuality
SIO_000300: 2.63419e5

QD
type: SiteQuality
SIO_000300: 3.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.86e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.818000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 317
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 188
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2630
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.626545217957059e-4
allele num: 6148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1508
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.0e-2

FS
type: SiteQuality
SIO_000300: 1.1184e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.84e0

DP
type: SiteQuality
SIO_000300: 2.63419e5

MQRankSum
type: SiteQuality
SIO_000300: 2.07e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.818000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.86e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.552e0

GenotypeQuality
all individuals: 238
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 450
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3054
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.852253280091272e-4
allele num: 7012
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 170
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.07e0

QD
type: SiteQuality
SIO_000300: 7.3e-1

DP
type: SiteQuality
SIO_000300: 2.69886e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 389
bin: 6.75e1
variant carriers: 15

GenotypeQuality
all individuals: 232
bin: 1.75e1
variant carriers: 17

GenotypeQuality
all individuals: 615
bin: 2.25e1
variant carriers: 16

GenotypeQuality
all individuals: 259
bin: 4.25e1
variant carriers: 14

GenotypeQuality
all individuals: 168
bin: 5.75e1
variant carriers: 11

GenotypeQuality
all individuals: 405
bin: 3.25e1
variant carriers: 19

GenotypeQuality
all individuals: 213
bin: 8.25e1
variant carriers: 6

GenotypeQuality
all individuals: 246
bin: 7.75e1
variant carriers: 10

GenotypeQuality
all individuals: 249
bin: 1.25e1
variant carriers: 24

GenotypeQuality
all individuals: 315
bin: 2.75e1
variant carriers: 8

Other
type: Population
allele count: 3
allele frequency: 2.238805970149254e-2
allele num: 134
num of homozygotes: 0

South Asian
type: Population
allele count: 109
allele frequency: 1.8722088629337e-2
allele num: 5822
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 73
allele frequency: 2.929373996789727e-2
allele num: 2492
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 2.941176470588235e-2
allele num: 136
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.09090909090909e-3
allele num: 110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 17
allele frequency: 1.32398753894081e-2
allele num: 1284
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 2.127659574468085e-2
allele num: 282
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.225e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-1

DP
type: SiteQuality
SIO_000300: 2.59716e5

FS
type: SiteQuality
SIO_000300: 3.1456e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.859e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.75e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-2

MQ
type: SiteQuality
SIO_000300: 6.008e1

QD
type: SiteQuality
SIO_000300: 9.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.3e-1

GenotypeQuality
all individuals: 997
bin: 2.5e0
variant carriers: 179

GenotypeQuality
all individuals: 166
bin: 9.25e1
variant carriers: 131

GenotypeQuality
all individuals: 270
bin: 1.75e1
variant carriers: 206

GenotypeQuality
all individuals: 201
bin: 6.25e1
variant carriers: 156

GenotypeQuality
all individuals: 2430
bin: 9.75e1
variant carriers: 1637

GenotypeQuality
all individuals: 215
bin: 2.75e1
variant carriers: 176

GenotypeQuality
all individuals: 142
bin: 8.75e1
variant carriers: 103

GenotypeQuality
all individuals: 156
bin: 8.25e1
variant carriers: 119

GenotypeQuality
all individuals: 209
bin: 5.75e1
variant carriers: 160

GenotypeQuality
all individuals: 189
bin: 5.25e1
variant carriers: 154

African
type: Population
allele count: 126
allele frequency: 3.962264150943396e-1
allele num: 318
num of homozygotes: 8

South Asian
type: Population
allele count: 1954
allele frequency: 3.395898505387556e-1
allele num: 5754
num of homozygotes: 28

Latino
type: Population
allele count: 39
allele frequency: 3.482142857142857e-1
allele num: 112
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 650
allele frequency: 4.716981132075472e-1
allele num: 1378
num of homozygotes: 59

European (Non-Finnish)
type: Population
allele count: 1125
allele frequency: 4.210329341317365e-1
allele num: 2672
num of homozygotes: 49

Other
type: Population
allele count: 59
allele frequency: 4.154929577464789e-1
allele num: 142
num of homozygotes: 4

East Asian
type: Population
allele count: 61
allele frequency: 4.013157894736842e-1
allele num: 152
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.0042e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.34e0

QD
type: SiteQuality
SIO_000300: 7.67e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.06e-1

African
type: Population
allele count: 38
allele frequency: 1.19496855345912e-1
allele num: 318
num of homozygotes: 0

Other
type: Population
allele count: 15
allele frequency: 1.056338028169014e-1
allele num: 142
num of homozygotes: 0

East Asian
type: Population
allele count: 17
allele frequency: 1.118421052631579e-1
allele num: 152
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

DP
type: SiteQuality
SIO_000300: 2.0042e5

QD
type: SiteQuality
SIO_000300: 7.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

GenotypeQuality
all individuals: 459
bin: 7.5e0
variant carriers: 14

GenotypeQuality
all individuals: 215
bin: 2.75e1
variant carriers: 12

GenotypeQuality
all individuals: 997
bin: 2.5e0
variant carriers: 20

GenotypeQuality
all individuals: 219
bin: 4.75e1
variant carriers: 10

GenotypeQuality
all individuals: 170
bin: 6.75e1
variant carriers: 7

GenotypeQuality
all individuals: 166
bin: 9.25e1
variant carriers: 10

GenotypeQuality
all individuals: 187
bin: 7.25e1
variant carriers: 11

GenotypeQuality
all individuals: 209
bin: 5.75e1
variant carriers: 14

GenotypeQuality
all individuals: 182
bin: 7.75e1
variant carriers: 5

GenotypeQuality
all individuals: 270
bin: 1.75e1
variant carriers: 12

European (Non-Finnish)
type: Population
allele count: 64
allele frequency: 2.395209580838323e-2
allele num: 2672
num of homozygotes: 1

South Asian
type: Population
allele count: 112
allele frequency: 1.94647201946472e-2
allele num: 5754
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 55
allele frequency: 3.991291727140784e-2
allele num: 1378
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.357142857142857e-2
allele num: 112
num of homozygotes: 0

African
type: Population
allele count: 29
allele frequency: 9.119496855345911e-2
allele num: 318
num of homozygotes: 1

East Asian
type: Population
allele count: 4
allele frequency: 2.631578947368421e-2
allele num: 152
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 1.408450704225352e-2
allele num: 142
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

QD
type: SiteQuality
SIO_000300: 7.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.0042e5

GenotypeQuality
all individuals: 206
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 215
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2430
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 7.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2672
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5754
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 7.25689404934688e-4
allele num: 1378
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.144654088050315e-3
allele num: 318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 142
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

QD
type: SiteQuality
SIO_000300: 7.67e0

DP
type: SiteQuality
SIO_000300: 2.0042e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

GenotypeQuality
all individuals: 182
bin: 7.75e1
variant carriers: 6

GenotypeQuality
all individuals: 235
bin: 3.25e1
variant carriers: 11

GenotypeQuality
all individuals: 236
bin: 2.25e1
variant carriers: 10

GenotypeQuality
all individuals: 156
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 142
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 166
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 5.25e1
variant carriers: 12

GenotypeQuality
all individuals: 201
bin: 6.25e1
variant carriers: 5

GenotypeQuality
all individuals: 187
bin: 7.25e1
variant carriers: 5

GenotypeQuality
all individuals: 170
bin: 6.75e1
variant carriers: 5

Latino
type: Population
allele count: 1
allele frequency: 8.928571428571428e-3
allele num: 112
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 7.042253521126761e-3
allele num: 142
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 2.515723270440252e-2
allele num: 318
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 6.578947368421052e-3
allele num: 152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 4.354136429608127e-3
allele num: 1378
num of homozygotes: 0

South Asian
type: Population
allele count: 41
allele frequency: 7.125477928397636e-3
allele num: 5754
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 40
allele frequency: 1.497005988023952e-2
allele num: 2672
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.0042e5

VQSLOD
type: SiteQuality
SIO_000300: 6.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.06e-1

QD
type: SiteQuality
SIO_000300: 7.67e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5754
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

DP
type: SiteQuality
SIO_000300: 2.0042e5

VQSLOD
type: SiteQuality
SIO_000300: 6.34e0

QD
type: SiteQuality
SIO_000300: 7.67e0

GenotypeQuality
all individuals: 2239
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 126
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 172
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.092145949288807e-4
allele num: 3234
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 172
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 370
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7088
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1590
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.45e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.881e0

FS
type: SiteQuality
SIO_000300: 5.478e0

QD
type: SiteQuality
SIO_000300: 3.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.28e-2

MQ
type: SiteQuality
SIO_000300: 6.039e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e0

MQRankSum
type: SiteQuality
SIO_000300: -1.524e0

DP
type: SiteQuality
SIO_000300: 1.92989e5

GenotypeQuality
all individuals: 288
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2914
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1152
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42595
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.137426900584795e-5
allele num: 10944
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.453e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.561389e6

VQSLOD
type: SiteQuality
SIO_000300: 3.08e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-1

QD
type: SiteQuality
SIO_000300: 9.66e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

GenotypeQuality
all individuals: 902
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 236
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3026
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42827
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1380
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7464
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11026
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 5.869692819409117e-4
allele num: 10222
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64592
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.77e-1

FS
type: SiteQuality
SIO_000300: 2.065e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.57e0

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.564062e6

QD
type: SiteQuality
SIO_000300: 1.506e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-1

GenotypeQuality
all individuals: 186
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 342
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7466
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1152
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 468
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11040
num of homozygotes: 0

East Asian
type: Population
allele count: 13
allele frequency: 1.513035381750465e-3
allele num: 8592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.325e1

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e-1

DP
type: SiteQuality
SIO_000300: 1.564722e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.49e-1

FS
type: SiteQuality
SIO_000300: 2.334e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.55e0

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 121
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7468
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11098
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.709284096847239e-5
allele num: 11482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64626
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.45e-1

FS
type: SiteQuality
SIO_000300: 3.039e0

DP
type: SiteQuality
SIO_000300: 1.565888e6

VQSLOD
type: SiteQuality
SIO_000300: 7.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.335e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.3e-1

QD
type: SiteQuality
SIO_000300: 1.196e1

GenotypeQuality
all individuals: 3032
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7504
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43632
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
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: 11506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64980
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
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: 1
allele frequency: 8.296001327360213e-5
allele num: 12054
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.464e0

QD
type: SiteQuality
SIO_000300: 1.481e1

VQSLOD
type: SiteQuality
SIO_000300: -6.567e-1

DP
type: SiteQuality
SIO_000300: 1.579365e6

MQRankSum
type: SiteQuality
SIO_000300: -1.219e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.87e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e0

GenotypeQuality
all individuals: 37
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1387
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 115
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 8.25e1
variant carriers: 2

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65164
num of homozygotes: 0

South Asian
type: Population
allele count: 13
allele frequency: 1.020087884494664e-3
allele num: 12744
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: 8620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQ
type: SiteQuality
SIO_000300: 5.949e1

QD
type: SiteQuality
SIO_000300: 1.245e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.25e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.71e-1

DP
type: SiteQuality
SIO_000300: 1.589686e6

VQSLOD
type: SiteQuality
SIO_000300: 9.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeQuality
all individuals: 7529
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1380
bin: 7.25e1
variant carriers: 3

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

GenotypeQuality
all individuals: 44200
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 163
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1058
bin: 9.75e1
variant carriers: 396

GenotypeQuality
all individuals: 2658
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 351
allele frequency: 5.382444948782433e-3
allele num: 65212
num of homozygotes: 1

Other
type: Population
allele count: 2
allele frequency: 2.369668246445498e-3
allele num: 844
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 23
allele frequency: 3.477472029029332e-3
allele num: 6614
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 1.071498149230469e-3
allele num: 10266
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.474635163307853e-4
allele num: 11512
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 8.537721204594847e-4
allele num: 12884
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-2

DP
type: SiteQuality
SIO_000300: 1.607047e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.71e-1

FS
type: SiteQuality
SIO_000300: 5.9e-1

QD
type: SiteQuality
SIO_000300: 1.3e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

GenotypeQuality
all individuals: 119
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 668
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 101
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 318
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1382
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13008
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.065885887727259e-5
allele num: 65234
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: 11516
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.96e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

FS
type: SiteQuality
SIO_000300: 9.553000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: -4.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.381e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

DP
type: SiteQuality
SIO_000300: 1.586878e6

QD
type: SiteQuality
SIO_000300: 1.435e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.99e-1

GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2486
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44784
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 668
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 296
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1389
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531065315246348e-5
allele num: 65314
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
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: 842
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10274
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.034e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.589885e6

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.69e-1

QD
type: SiteQuality
SIO_000300: 1.218e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46153
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.557054320087495e-5
allele num: 65832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
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: 14710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.155e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.612653e6

VQSLOD
type: SiteQuality
SIO_000300: 4.84e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

QD
type: SiteQuality
SIO_000300: 1.277e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.12e-1

GenotypeQuality
all individuals: 131
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1316
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 122
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1072
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 8.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 315
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 46084
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 181
allele frequency: 1.215417673918883e-2
allele num: 14892
num of homozygotes: 2

African
type: Population
allele count: 490
allele frequency: 4.743465634075508e-2
allele num: 10330
num of homozygotes: 13

Other
type: Population
allele count: 6
allele frequency: 6.880733944954129e-3
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 477
allele frequency: 7.237800436999272e-3
allele num: 65904
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 12
allele frequency: 1.814333232537043e-3
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 62
allele frequency: 5.368895046761344e-3
allele num: 11548
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.44e-1

DP
type: SiteQuality
SIO_000300: 1.666712e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.67e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.79e-1

QD
type: SiteQuality
SIO_000300: 1.207e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.98e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

GenotypeQuality
all individuals: 97
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7825
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47256
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 7
allele frequency: 6.777691711851278e-4
allele num: 10328
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158480074142725e-4
allele num: 8632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65986
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15158
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
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: 8.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

QD
type: SiteQuality
SIO_000300: 1.321e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-2

FS
type: SiteQuality
SIO_000300: 2.517e0

MQRankSum
type: SiteQuality
SIO_000300: -1.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.46e-1

DP
type: SiteQuality
SIO_000300: 1.603677e6

MQ
type: SiteQuality
SIO_000300: 5.921e1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

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

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

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 687
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 385
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1112
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66248
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
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: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15900
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.916e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.809e0

MQRankSum
type: SiteQuality
SIO_000300: -8.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.045e1

FS
type: SiteQuality
SIO_000300: 8.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.299e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

DP
type: SiteQuality
SIO_000300: 1.61493e6

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 105
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 9.75e1
variant carriers: 5

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.036278030966107e-5
allele num: 66266
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: 10332
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.263309532757109e-5
allele num: 15966
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: 898
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.182e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.97e-1

FS
type: SiteQuality
SIO_000300: 4.968e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

MQ
type: SiteQuality
SIO_000300: 5.944e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

DP
type: SiteQuality
SIO_000300: 1.617457e6

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1411
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7924
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48234
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.22975330176925e-5
allele num: 16052
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.507658907248824e-4
allele num: 66328
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: 10338
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.731301939058172e-4
allele num: 11552
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.618989e6

MQ
type: SiteQuality
SIO_000300: 5.94e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-1

QD
type: SiteQuality
SIO_000300: 1.165e1

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-2

FS
type: SiteQuality
SIO_000300: 5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 102
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1412
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7935
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16182
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: 904
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.671179883945841e-5
allele num: 10340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66388
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.621788e6

VQSLOD
type: SiteQuality
SIO_000300: -1.677e0

FS
type: SiteQuality
SIO_000300: 1.2627e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.544e0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.41e-1

QD
type: SiteQuality
SIO_000300: 1.065e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.4e-2

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7986
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.009147809340395e-5
allele num: 66464
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: 2
allele frequency: 3.023888720895071e-4
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16370
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.39e-1

QD
type: SiteQuality
SIO_000300: 9.73e0

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

DP
type: SiteQuality
SIO_000300: 1.62538e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

VQSLOD
type: SiteQuality
SIO_000300: 7.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.761e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7992
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 386
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66476
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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.028e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e0

QD
type: SiteQuality
SIO_000300: 1.203e1

MQ
type: SiteQuality
SIO_000300: 5.936e1

FS
type: SiteQuality
SIO_000300: 6.011e0

VQSLOD
type: SiteQuality
SIO_000300: -8.621e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

DP
type: SiteQuality
SIO_000300: 1.626002e6

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49003
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504030802550836e-5
allele num: 66488
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: 6606
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: 2
allele frequency: 2.318034306907742e-4
allele num: 8628
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

FS
type: SiteQuality
SIO_000300: 1.519e0

QD
type: SiteQuality
SIO_000300: 1.394e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.65e-1

DP
type: SiteQuality
SIO_000300: 1.627031e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.93e-1

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1095
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1398
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 321
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.477857639693948e-4
allele num: 8626
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: 66472
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 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: 11546
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.2e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.502e0

FS
type: SiteQuality
SIO_000300: 1.31e0

MQRankSum
type: SiteQuality
SIO_000300: -3.74e-1

QD
type: SiteQuality
SIO_000300: 1.096e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.626774e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.69e-1

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7966
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
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: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.53e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

DP
type: SiteQuality
SIO_000300: 1.625818e6

MQ
type: SiteQuality
SIO_000300: 5.903e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 9.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.8e0

QD
type: SiteQuality
SIO_000300: 1.207e1

VQSLOD
type: SiteQuality
SIO_000300: -6.7e-3

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 48978
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1392
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7959
bin: 6.75e1
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: 6602
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.5e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.86e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.068e0

QD
type: SiteQuality
SIO_000300: 8.369999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.482e1

DP
type: SiteQuality
SIO_000300: 1.625431e6

GenotypeQuality
all individuals: 74
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1389
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7942
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48861
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.670019074041963e-5
allele num: 11534
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505615947484116e-5
allele num: 66418
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.62457e6

MQRankSum
type: SiteQuality
SIO_000300: 1.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.748e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.01e0

QD
type: SiteQuality
SIO_000300: 1.568e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.43e-1

GenotypeQuality
all individuals: 737
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
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: 1.165501165501166e-4
allele num: 8580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0