http://identifiers.org/exac.variant/19-42599820-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599820
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599820
    reference: chr 19
allele count: 2
allele frequency: 1.696410395602904e-5
allele num: 117896
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.831G>T
  hgvsp: ENST00000529952.1:c.831G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.849G>T
  hgvsp: ENST00000560398.1:c.849G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.831G>T
  hgvsp: ENST00000342301.4:c.831G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.666G>T
  hgvsp: ENST00000560558.1:c.666G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.831G>T
  hgvsp: ENST00000526816.2:c.831G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.837G>T
  hgvsp: ENST00000560804.2:c.837G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*592G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.783G>T
  hgvsp: ENST00000529067.1:c.783G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.783G>T
  hgvsp: ENST00000389341.5:c.783G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.783G>T
  hgvsp: ENST00000533720.1:c.783G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu277Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD

19-42599837-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599837
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599837
    reference: chr 19
allele count: 1
allele frequency: 8.457660949287865e-6
allele num: 118236
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.814T>C
  hgvsp: ENSP00000431603.3:p.Ser272Pro
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*575T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.832T>C
  hgvsp: ENSP00000453255.1:p.Ser278Pro
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.649T>C
  hgvsp: ENSP00000454179.1:p.Ser217Pro
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.820T>C
  hgvsp: ENSP00000452930.2:p.Ser274Pro
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.766T>C
  hgvsp: ENSP00000437221.1:p.Ser256Pro
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.814T>C
  hgvsp: ENSP00000436988.1:p.Ser272Pro
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.766T>C
  hgvsp: ENSP00000437224.1:p.Ser256Pro
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.814T>C
  hgvsp: ENSP00000339369.4:p.Ser272Pro
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.766T>C
  hgvsp: ENSP00000373992.3:p.Ser256Pro
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser272Pro
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/19-42599841-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599841
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599841
    reference: chr 19
allele count: 1
allele frequency: 8.456516591685553e-6
allele num: 118252
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.762T>G
  hgvsp: ENST00000529067.1:c.762T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.762T>G
  hgvsp: ENST00000533720.1:c.762T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.645T>G
  hgvsp: ENST00000560558.1:c.645T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*571T>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.762T>G
  hgvsp: ENST00000389341.5:c.762T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.810T>G
  hgvsp: ENST00000526816.2:c.810T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.816T>G
  hgvsp: ENST00000560804.2:c.816T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.810T>G
  hgvsp: ENST00000529952.1:c.810T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.810T>G
  hgvsp: ENST00000342301.4:c.810T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.828T>G
  hgvsp: ENST00000560398.1:c.828T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 1
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: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1684
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr270Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

19-42599841-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599841
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599841
    reference: chr 19
allele count: 2
allele frequency: 1.691303318337111e-5
allele num: 118252
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.810T>C
  hgvsp: ENST00000529952.1:c.810T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.762T>C
  hgvsp: ENST00000533720.1:c.762T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.645T>C
  hgvsp: ENST00000560558.1:c.645T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.762T>C
  hgvsp: ENST00000529067.1:c.762T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.816T>C
  hgvsp: ENST00000560804.2:c.816T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.762T>C
  hgvsp: ENST00000389341.5:c.762T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.810T>C
  hgvsp: ENST00000526816.2:c.810T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*571T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.828T>C
  hgvsp: ENST00000560398.1:c.828T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.810T>C
  hgvsp: ENST00000342301.4:c.810T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30678
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr270Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

19-42599852-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599852
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599852
    reference: chr 19
allele count: 93
allele frequency: 7.875082561349434e-4
allele num: 118094
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.806-7C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.758-7C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.758-7C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.758-7C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.806-7C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.641-7C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*567-7C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.806-7C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.812-7C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.824-7C>T
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 18588
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 3.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30001
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 3.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 2548
  bin: 2.25e1
  variant carriers: 0
hgvs: c.806-7C>T
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

19-42599852-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599852
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599852
    reference: chr 19
allele count: 1
allele frequency: 8.467830711128423e-6
allele num: 118094
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.812-7C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.758-7C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.806-7C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.824-7C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.758-7C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.806-7C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.641-7C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*567-7C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.758-7C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.806-7C>A
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42448
  bin: 6.25e1
  variant carriers: 0
hgvs: c.806-7C>A
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

19-42599853-CCGGGG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599853
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599848
    reference: chr 19
allele count: 4
allele frequency: 3.387533875338753e-5
allele num: 118080
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.812-13_812-9delCCCCG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.806-13_806-9delCCCCG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.641-13_641-9delCCCCG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.758-13_758-9delCCCCG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.758-13_758-9delCCCCG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*567-13_*567-9delCCCCG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.806-13_806-9delCCCCG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.758-13_758-9delCCCCG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.806-13_806-9delCCCCG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.824-13_824-9delCCCCG
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 1.75e1
  variant carriers: 2
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: 19
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29936
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 858
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: CCGGGG
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-42599855-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599855
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599855
    reference: chr 19
allele count: 3
allele frequency: 2.541123854376662e-5
allele num: 118058
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.824-10C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.806-10C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.758-10C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.758-10C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.812-10C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.758-10C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.641-10C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*567-10C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.806-10C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.806-10C>T
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff

19-42599858-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599858
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599858
    reference: chr 19
allele count: 1
allele frequency: 8.457517887650332e-6
allele num: 118238
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.806-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*567-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.758-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.758-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.806-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.806-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.824-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.641-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.758-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.812-13C>T
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  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: 210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

19-42599858-G-GAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599858
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599860
    reference: chr 19
allele count: 4
allele frequency: 3.383007155060133e-5
allele num: 118238
alternate allele: GAT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.806-14_806-13insAT
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.758-14_758-13insAT
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.812-14_812-13insAT
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.824-14_824-13insAT
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*567-14_*567-13insAT
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.806-14_806-13insAT
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.758-14_758-13insAT
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.806-14_806-13insAT
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.641-14_641-13insAT
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.758-14_758-13insAT
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6238
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

19-42599859-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599859
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599859
    reference: chr 19
allele count: 2
allele frequency: 1.691074508742855e-5
allele num: 118268
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*567-14C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.758-14C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.641-14C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.758-14C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.758-14C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.806-14C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.824-14C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.806-14C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.806-14C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.812-14C>T
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43516
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-42599880-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599880
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599880
    reference: chr 19
allele count: 1
allele frequency: 8.458948721852847e-6
allele num: 118218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.641-35C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.758-35C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.806-35C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.824-35C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.806-35C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.812-35C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*567-35C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.806-35C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.758-35C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.758-35C>T
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5660
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1749
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

19-42599886-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599886
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599886
    reference: chr 19
allele count: 1
allele frequency: 8.454228805248384e-6
allele num: 118284
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*567-41G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.758-41G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.806-41G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.806-41G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.812-41G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.758-41G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.824-41G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.641-41G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.758-41G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.806-41G>C
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5841
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29070
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ

19-42599888-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599888
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599888
    reference: chr 19
allele count: 1
allele frequency: 8.495599279573181e-6
allele num: 117708
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.806-43G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.758-43G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*567-43G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.758-43G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.806-43G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.812-43G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.806-43G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.758-43G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.824-43G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.641-43G>C
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6096
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1951
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP

19-42599889-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599889
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599889
    reference: chr 19
allele count: 1
allele frequency: 8.459807454782329e-6
allele num: 118206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.758-44C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.806-44C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.806-44C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.758-44C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*567-44C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.812-44C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.758-44C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.806-44C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.641-44C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.824-44C>T
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 917
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1708
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

19-42599895-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599895
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599895
    reference: chr 19
allele count: 25
allele frequency: 2.103668798384382e-4
allele num: 118840
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*566+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.757+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.811+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.805+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.805+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.640+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.823+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.757+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.757+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.805+45G>A
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6498
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28309
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1742
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP

19-42599896-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599896
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599896
    reference: chr 19
allele count: 2
allele frequency: 1.679345726904798e-5
allele num: 119094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.640+44C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.823+44C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.805+44C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.811+44C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.757+44C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.805+44C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.757+44C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*566+44C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.805+44C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.757+44C>T
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  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: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6577
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

19-42599906-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599906
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599906
    reference: chr 19
allele count: 1
allele frequency: 8.378156470450242e-6
allele num: 119358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.811+34G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.805+34G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.805+34G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*566+34G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.640+34G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.805+34G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.757+34G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.757+34G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.757+34G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.823+34G>A
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45931
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

19-42599907-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599907
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599908
    reference: chr 19
allele count: 1
allele frequency: 8.369601606963508e-6
allele num: 119480
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.811+32dupG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*566+32dupG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.640+32dupG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.805+32dupG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.757+32dupG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.757+32dupG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.757+32dupG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.805+32dupG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.823+32dupG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.805+32dupG
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

19-42599916-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599916
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599916
    reference: chr 19
allele count: 1
allele frequency: 8.336807002917883e-6
allele num: 119950
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.805+24C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.805+24C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*566+24C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.640+24C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.805+24C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.757+24C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.757+24C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.757+24C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.823+24C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.811+24C>T
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6796
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

19-42599929-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599929
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599929
    reference: chr 19
allele count: 1
allele frequency: 8.288987251537607e-6
allele num: 120642
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.805+11G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.823+11G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.805+11G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.640+11G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.757+11G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.811+11G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.757+11G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.805+11G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*566+11G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.757+11G>A
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6926
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

19-42599931-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599931
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599931
    reference: chr 19
allele count: 2
allele frequency: 1.65694591728526e-5
allele num: 120704
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.805+9A>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.757+9A>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*566+9A>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.757+9A>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.640+9A>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.805+9A>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.757+9A>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.823+9A>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.811+9A>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.805+9A>T
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  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 quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1847
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum

19-42599935-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599935
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599935
    reference: chr 19
allele count: 1
allele frequency: 8.275542461808372e-6
allele num: 120838
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.640+5G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.757+5G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.811+5G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.823+5G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*566+5G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.805+5G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.757+5G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.805+5G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.757+5G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.805+5G>C
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48354
  bin: 6.25e1
  variant carriers: 0
hgvs: c.805+5G>C
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

19-42599935-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599935
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599935
    reference: chr 19
allele count: 1
allele frequency: 8.275542461808372e-6
allele num: 120838
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.811+5G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.805+5G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.805+5G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.757+5G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.805+5G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.757+5G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.640+5G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*566+5G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.757+5G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.823+5G>A
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48354
  bin: 6.25e1
  variant carriers: 0
hgvs: c.805+5G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS

19-42599944-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599944
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599944
    reference: chr 19
allele count: 4
allele frequency: 3.304092118088253e-5
allele num: 121062
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.801T>C
  hgvsp: ENST00000342301.4:c.801T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.753T>C
  hgvsp: ENST00000389341.5:c.753T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.781T>C
  hgvsp: ENST00000528894.4:c.781T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.636T>C
  hgvsp: ENST00000560558.1:c.636T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*562T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.801T>C
  hgvsp: ENST00000526816.2:c.801T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.807T>C
  hgvsp: ENST00000560804.2:c.807T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.801T>C
  hgvsp: ENST00000529952.1:c.801T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.819T>C
  hgvsp: ENST00000560398.1:c.819T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.753T>C
  hgvsp: ENST00000533720.1:c.753T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.753T>C
  hgvsp: ENST00000529067.1:c.753T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21988
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp267Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

19-42599946-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599946
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599946
    reference: chr 19
allele count: 2
allele frequency: 1.65174589541145e-5
allele num: 121084
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.779G>A
  hgvsp: ENSP00000475664.1:p.Asp261Asn
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.817G>A
  hgvsp: ENSP00000453255.1:p.Asp273Asn
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.799G>A
  hgvsp: ENSP00000436988.1:p.Asp267Asn
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.799G>A
  hgvsp: ENSP00000431603.3:p.Asp267Asn
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.751G>A
  hgvsp: ENSP00000437221.1:p.Asp251Asn
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.634G>A
  hgvsp: ENSP00000454179.1:p.Asp212Asn
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.751G>A
  hgvsp: ENSP00000373992.3:p.Asp251Asn
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.799G>A
  hgvsp: ENSP00000339369.4:p.Asp267Asn
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.805G>A
  hgvsp: ENSP00000452930.2:p.Asp269Asn
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.751G>A
  hgvsp: ENSP00000437224.1:p.Asp251Asn
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*560G>A
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp267Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

19-42599947-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599947
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599947
    reference: chr 19
allele count: 1
allele frequency: 8.256274768824306e-6
allele num: 121120
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.816C>T
  hgvsp: ENST00000560398.1:c.816C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.798C>T
  hgvsp: ENST00000529952.1:c.798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.804C>T
  hgvsp: ENST00000560804.2:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.778C>T
  hgvsp: ENST00000528894.4:c.778C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.798C>T
  hgvsp: ENST00000526816.2:c.798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.798C>T
  hgvsp: ENST00000342301.4:c.798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*559C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.750C>T
  hgvsp: ENST00000529067.1:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.750C>T
  hgvsp: ENST00000389341.5:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.633C>T
  hgvsp: ENST00000560558.1:c.633C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.750C>T
  hgvsp: ENST00000533720.1:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn266Asn
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

19-42599948-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599948
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599948
    reference: chr 19
allele count: 2
allele frequency: 1.651173158529135e-5
allele num: 121126
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.797A>G
  hgvsp: ENSP00000436988.1:p.Asn266Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.797A>G
  hgvsp: ENSP00000431603.3:p.Asn266Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.777A>G
  hgvsp: ENSP00000475664.1:p.Asn260Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.803A>G
  hgvsp: ENSP00000452930.2:p.Asn268Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*558A>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.749A>G
  hgvsp: ENSP00000437224.1:p.Asn250Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.815A>G
  hgvsp: ENSP00000453255.1:p.Asn272Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.749A>G
  hgvsp: ENSP00000373992.3:p.Asn250Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.632A>G
  hgvsp: ENSP00000454179.1:p.Asn211Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.749A>G
  hgvsp: ENSP00000437221.1:p.Asn250Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.797A>G
  hgvsp: ENSP00000339369.4:p.Asn266Ser
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn266Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

19-42599950-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599950
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599950
    reference: chr 19
allele count: 1
allele frequency: 8.254502831294471e-6
allele num: 121146
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.795C>T
  hgvsp: ENST00000529952.1:c.795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.747C>T
  hgvsp: ENST00000529067.1:c.747C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.795C>T
  hgvsp: ENST00000342301.4:c.795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.630C>T
  hgvsp: ENST00000560558.1:c.630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.813C>T
  hgvsp: ENST00000560398.1:c.813C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.795C>T
  hgvsp: ENST00000526816.2:c.795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.775C>T
  hgvsp: ENST00000528894.4:c.775C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*556C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.747C>T
  hgvsp: ENST00000389341.5:c.747C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.747C>T
  hgvsp: ENST00000533720.1:c.747C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.801C>T
  hgvsp: ENST00000560804.2:c.801C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  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: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu265Leu
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS

19-42599959-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599959
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599959
    reference: chr 19
allele count: 7
allele frequency: 5.774910488887422e-5
allele num: 121214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.786G>A
  hgvsp: ENST00000342301.4:c.786G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.786G>A
  hgvsp: ENST00000529952.1:c.786G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.738G>A
  hgvsp: ENST00000533720.1:c.738G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.621G>A
  hgvsp: ENST00000560558.1:c.621G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.766G>A
  hgvsp: ENST00000528894.4:c.766G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.786G>A
  hgvsp: ENST00000526816.2:c.786G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.804G>A
  hgvsp: ENST00000560398.1:c.804G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.792G>A
  hgvsp: ENST00000560804.2:c.792G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.738G>A
  hgvsp: ENST00000529067.1:c.738G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.738G>A
  hgvsp: ENST00000389341.5:c.738G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*547G>A
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6852
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu262Glu
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

19-42599965-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599965
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599965
    reference: chr 19
allele count: 2
allele frequency: 1.649348507339601e-5
allele num: 121260
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.786C>G
  hgvsp: ENST00000560804.2:c.786C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.760C>G
  hgvsp: ENST00000528894.4:c.760C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.780C>G
  hgvsp: ENST00000342301.4:c.780C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.732C>G
  hgvsp: ENST00000529067.1:c.732C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*541C>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.780C>G
  hgvsp: ENST00000529952.1:c.780C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.780C>G
  hgvsp: ENST00000526816.2:c.780C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.732C>G
  hgvsp: ENST00000389341.5:c.732C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.615C>G
  hgvsp: ENST00000560558.1:c.615C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.798C>G
  hgvsp: ENST00000560398.1:c.798C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.732C>G
  hgvsp: ENST00000533720.1:c.732C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.656C>G
  hgvsp: ENST00000526831.1:c.656C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu260Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

19-42599968-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599968
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599968
    reference: chr 19
allele count: 11
allele frequency: 9.069621714323406e-5
allele num: 121284
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.612C>G
  hgvsp: ENST00000560558.1:c.612C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.777C>G
  hgvsp: ENST00000529952.1:c.777C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.777C>G
  hgvsp: ENST00000342301.4:c.777C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.729C>G
  hgvsp: ENST00000533720.1:c.729C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.653C>G
  hgvsp: ENST00000526831.1:c.653C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.757C>G
  hgvsp: ENST00000528894.4:c.757C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.777C>G
  hgvsp: ENST00000526816.2:c.777C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.729C>G
  hgvsp: ENST00000389341.5:c.729C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.795C>G
  hgvsp: ENST00000560398.1:c.795C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.783C>G
  hgvsp: ENST00000560804.2:c.783C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*538C>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.729C>G
  hgvsp: ENST00000529067.1:c.729C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22082
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro259Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

19-42599971-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599971
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599971
    reference: chr 19
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.726G>A
  hgvsp: ENST00000533720.1:c.726G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.774G>A
  hgvsp: ENST00000342301.4:c.774G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.774G>A
  hgvsp: ENST00000529952.1:c.774G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.754G>A
  hgvsp: ENST00000528894.4:c.754G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.726G>A
  hgvsp: ENST00000529067.1:c.726G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.780G>A
  hgvsp: ENST00000560804.2:c.780G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.650G>A
  hgvsp: ENST00000526831.1:c.650G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.792G>A
  hgvsp: ENST00000560398.1:c.792G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*535G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.609G>A
  hgvsp: ENST00000560558.1:c.609G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.774G>A
  hgvsp: ENST00000526816.2:c.774G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.726G>A
  hgvsp: ENST00000389341.5:c.726G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys258Lys
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP

19-42599995-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42599995
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42599995
    reference: chr 19
allele count: 190
allele frequency: 1.565925461948011e-3
allele num: 121334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.768C>T
  hgvsp: ENST00000560398.1:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.750C>T
  hgvsp: ENST00000526816.2:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.585C>T
  hgvsp: ENST00000560558.1:c.585C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.756C>T
  hgvsp: ENST00000560804.2:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.702C>T
  hgvsp: ENST00000533720.1:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.750C>T
  hgvsp: ENST00000342301.4:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.626C>T
  hgvsp: ENST00000526831.1:c.626C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.730C>T
  hgvsp: ENST00000528894.4:c.730C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.702C>T
  hgvsp: ENST00000529067.1:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.702C>T
  hgvsp: ENST00000389341.5:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*511C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.750C>T
  hgvsp: ENST00000529952.1:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 147
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 22063
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser250Ser
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ

19-42600013-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600013
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600013
    reference: chr 19
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.712C>T
  hgvsp: ENST00000528894.4:c.712C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.750C>T
  hgvsp: ENST00000560398.1:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.684C>T
  hgvsp: ENST00000389341.5:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.732C>T
  hgvsp: ENST00000529952.1:c.732C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.732C>T
  hgvsp: ENST00000342301.4:c.732C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.738C>T
  hgvsp: ENST00000560804.2:c.738C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*493C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.567C>T
  hgvsp: ENST00000560558.1:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.732C>T
  hgvsp: ENST00000526816.2:c.732C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.684C>T
  hgvsp: ENST00000533720.1:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.608C>T
  hgvsp: ENST00000526831.1:c.608C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.684C>T
  hgvsp: ENST00000529067.1:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29913
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe244Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

19-42600024-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600024
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600024
    reference: chr 19
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.739A>G
  hgvsp: ENSP00000453255.1:p.Ile247Val
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.721A>G
  hgvsp: ENSP00000431603.3:p.Ile241Val
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.556A>G
  hgvsp: ENSP00000454179.1:p.Ile186Val
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.673A>G
  hgvsp: ENSP00000437221.1:p.Ile225Val
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.597A>G
  hgvsp: ENSP00000476062.1:p.Ile200Val
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.721A>G
  hgvsp: ENSP00000339369.4:p.Ile241Val
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.673A>G
  hgvsp: ENSP00000373992.3:p.Ile225Val
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.701A>G
  hgvsp: ENSP00000475664.1:p.Ile235Val
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.727A>G
  hgvsp: ENSP00000452930.2:p.Ile243Val
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*482A>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.721A>G
  hgvsp: ENSP00000436988.1:p.Ile241Val
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.673A>G
  hgvsp: ENSP00000437224.1:p.Ile225Val
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.75e1
  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: 1
genotype depth: GenotypeDepth
  all individuals: 29883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22088
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile241Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-42600052-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600052
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600052
    reference: chr 19
allele count: 42
allele frequency: 3.472222222222222e-4
allele num: 120960
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.699C>T
  hgvsp: ENST00000560804.2:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.645C>T
  hgvsp: ENST00000529067.1:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.693C>T
  hgvsp: ENST00000526816.2:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.645C>T
  hgvsp: ENST00000389341.5:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.693C>T
  hgvsp: ENST00000342301.4:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.645C>T
  hgvsp: ENST00000533720.1:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.673C>T
  hgvsp: ENST00000528894.4:c.673C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.693C>T
  hgvsp: ENST00000529952.1:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*454C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.711C>T
  hgvsp: ENST00000560398.1:c.711C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.528C>T
  hgvsp: ENST00000560558.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.569C>T
  hgvsp: ENST00000526831.1:c.569C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29294
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21871
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6862
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Leu231Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/19-42600066-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600066
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600066
    reference: chr 19
allele count: 1
allele frequency: 8.300683976359652e-6
allele num: 120472
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.631G>T
  hgvsp: ENSP00000437221.1:p.Ala211Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.659G>T
  hgvsp: ENSP00000475664.1:p.Ala221Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.679G>T
  hgvsp: ENSP00000339369.4:p.Ala227Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*440G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.679G>T
  hgvsp: ENSP00000431603.3:p.Ala227Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.514G>T
  hgvsp: ENSP00000454179.1:p.Ala172Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.679G>T
  hgvsp: ENSP00000436988.1:p.Ala227Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.555G>T
  hgvsp: ENSP00000476062.1:p.Ala186Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.631G>T
  hgvsp: ENSP00000437224.1:p.Ala211Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.685G>T
  hgvsp: ENSP00000452930.2:p.Ala229Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.697G>T
  hgvsp: ENSP00000453255.1:p.Ala233Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.631G>T
  hgvsp: ENSP00000373992.3:p.Ala211Ser
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala227Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

19-42600089-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600089
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600089
    reference: chr 19
allele count: 1
allele frequency: 8.382510729613734e-6
allele num: 119296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.616-8T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.670-8T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.682-8T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.540-8T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.644-8T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*425-8T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.616-8T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.664-8T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.664-8T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.664-8T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.616-8T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.499-8T>C
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
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: 26788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.664-8T>C
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: A
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

19-42600092-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600092
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600092
    reference: chr 19
allele count: 1
allele frequency: 8.393627557957998e-6
allele num: 119138
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.540-11C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.616-11C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.664-11C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.682-11C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.616-11C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.499-11C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.644-11C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.664-11C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*425-11C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.670-11C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.616-11C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.664-11C>T
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  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: 1
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

19-42600094-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600094
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600094
    reference: chr 19
allele count: 1
allele frequency: 8.420485356775965e-6
allele num: 118758
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.616-13C>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.616-13C>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.540-13C>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.664-13C>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.664-13C>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*425-13C>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.499-13C>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.644-13C>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.616-13C>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.682-13C>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.670-13C>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.664-13C>G
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6721
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  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: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

19-42600094-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600094
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600094
    reference: chr 19
allele count: 3
allele frequency: 2.526145607032789e-5
allele num: 118758
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.664-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.540-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.664-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.670-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.616-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*425-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.616-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.499-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.644-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.682-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.616-13C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.664-13C>T
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

19-42600096-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600096
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600096
    reference: chr 19
allele count: 1
allele frequency: 8.435117079425063e-6
allele num: 118552
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.670-15G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.644-15G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.616-15G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.664-15G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.616-15G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*425-15G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.540-15G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.682-15G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.499-15G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.664-15G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.664-15G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.616-15G>A
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20581
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

19-42600101-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600101
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600101
    reference: chr 19
allele count: 1
allele frequency: 8.465250148141878e-6
allele num: 118130
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.664-20T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.664-20T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.664-20T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.616-20T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*425-20T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.499-20T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.644-20T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.682-20T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.616-20T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.540-20T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.670-20T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.616-20T>C
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6675
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-42600102-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600102
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600102
    reference: chr 19
allele count: 2
allele frequency: 1.693078694297711e-5
allele num: 118128
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.664-21T>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.616-21T>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.682-21T>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.540-21T>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.670-21T>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*425-21T>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.664-21T>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.644-21T>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.499-21T>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.616-21T>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.616-21T>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.664-21T>A
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20226
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3506
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6680
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

19-42600103-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600103
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600103
    reference: chr 19
allele count: 9
allele frequency: 7.620144274731602e-5
allele num: 118108
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.682-22C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.616-22C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.499-22C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.540-22C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.664-22C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.670-22C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.616-22C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.616-22C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.664-22C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.644-22C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*425-22C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.664-22C>T
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25508
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

19-42600104-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600104
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600104
    reference: chr 19
allele count: 7
allele frequency: 5.930293634253376e-5
allele num: 118038
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.540-23C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.664-23C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.664-23C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.664-23C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.644-23C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.616-23C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.616-23C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.616-23C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.670-23C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.499-23C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*425-23C>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.682-23C>A
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  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: 1381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25443
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6663
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

19-42600107-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600107
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600107
    reference: chr 19
allele count: 1
allele frequency: 8.496609852668785e-6
allele num: 117694
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.540-26G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.616-26G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.664-26G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.644-26G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.682-26G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.670-26G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.616-26G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.664-26G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*425-26G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.616-26G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.499-26G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.664-26G>A
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19937
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

19-42600112-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600112
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600112
    reference: chr 19
allele count: 46
allele frequency: 3.925651572820837e-4
allele num: 117178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.616-31C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.670-31C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.540-31C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.616-31C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.644-31C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*425-31C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.664-31C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.664-31C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.499-31C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.682-31C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.616-31C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.664-31C>T
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4569
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6544
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19256
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24346
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 4
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: 81
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

19-42600118-G-GTGGGGCCTTCCGGCAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600118
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600134
    reference: chr 19
allele count: 3
allele frequency: 2.571399184009326e-5
allele num: 116668
alternate allele: GTGGGGCCTTCCGGCAC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3677
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18252
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23126
  bin: 2.25e1
  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: 1138
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6400
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38371
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

19-42600124-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600124
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600124
    reference: chr 19
allele count: 3
allele frequency: 2.598077422707197e-5
allele num: 115470
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.670-43G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.499-43G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.664-43G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.664-43G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.540-43G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.644-43G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*425-43G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.682-43G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.616-43G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.616-43G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.616-43G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.664-43G>A
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22893
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-42600128-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600128
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600128
    reference: chr 19
allele count: 2
allele frequency: 1.741341180977589e-5
allele num: 114854
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.499-47G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.664-47G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*425-47G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.644-47G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.540-47G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.664-47G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.616-47G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.682-47G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.616-47G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.664-47G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.616-47G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.670-47G>T
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6993
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4970
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

19-42600129-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600129
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600129
    reference: chr 19
allele count: 3
allele frequency: 2.6279367192838e-5
allele num: 114158
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.616-48G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.616-48G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*425-48G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.644-48G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.664-48G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.499-48G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.670-48G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.616-48G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.664-48G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.664-48G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.540-48G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.682-48G>C
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6950
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4953
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/19-42600133-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600133
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600133
    reference: chr 19
allele count: 1
allele frequency: 8.877683279771311e-6
allele num: 112642
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.670-52T>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.499-52T>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.540-52T>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.664-52T>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.664-52T>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.616-52T>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.664-52T>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.682-52T>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.616-52T>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.644-52T>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.616-52T>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*425-52T>G
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

19-42600185-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600185
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600185
    reference: chr 19
allele count: 1
allele frequency: 9.304056568663937e-6
allele num: 107480
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.498+49G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.663+49G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.615+49G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*424+49G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.643+49G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.615+49G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.663+49G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.615+49G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.681+49G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.669+49G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.539+49G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.663+49G>A
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13270
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

19-42600189-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600189
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600189
    reference: chr 19
allele count: 1
allele frequency: 9.537798294641664e-6
allele num: 104846
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.663+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.498+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.615+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.663+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.615+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*424+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.643+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.663+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.539+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.681+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.615+45G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.669+45G>A
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11090
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13013
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14831
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-42600191-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600191
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600191
    reference: chr 19
allele count: 1
allele frequency: 9.478313618441007e-6
allele num: 105504
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.643+43T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*424+43T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.663+43T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.669+43T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.498+43T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.663+43T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.615+43T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.539+43T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.663+43T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.615+43T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.615+43T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.681+43T>C
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11042
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14620
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5843
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13066
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS

19-42600193-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600193
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600192
    reference: chr 19
allele count: 5
allele frequency: 4.740684554849721e-5
allele num: 105470
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.498+40delG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.663+40delG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.669+40delG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*424+40delG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.663+40delG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.615+40delG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.615+40delG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.663+40delG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.539+40delG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.643+40delG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.615+40delG
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.681+40delG
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13044
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5911
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11384
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11251
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14309
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: GC
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/19-42600200-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600200
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600200
    reference: chr 19
allele count: 1
allele frequency: 9.462886558915933e-6
allele num: 105676
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.498+34G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.643+34G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.663+34G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.539+34G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.615+34G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.663+34G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.681+34G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*424+34G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.669+34G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.663+34G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.615+34G>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.615+34G>T
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12854
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12786
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP

19-42600207-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600207
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600207
    reference: chr 19
allele count: 1
allele frequency: 9.394611250986435e-6
allele num: 106444
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.669+27G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.681+27G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.663+27G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.615+27G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.498+27G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*424+27G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.643+27G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.539+27G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.663+27G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.615+27G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.615+27G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.663+27G>A
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  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: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11030
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD

19-42600208-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600208
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600208
    reference: chr 19
allele count: 1
allele frequency: 9.420098722634613e-6
allele num: 106156
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.615+26C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.663+26C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.615+26C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.615+26C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.643+26C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.498+26C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.669+26C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*424+26C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.663+26C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.663+26C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.539+26C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.681+26C>T
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10488
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12159
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-42600213-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600213
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600213
    reference: chr 19
allele count: 1
allele frequency: 9.281603861147206e-6
allele num: 107740
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.643+21C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.669+21C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.663+21C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*424+21C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.498+21C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.615+21C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.663+21C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.615+21C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.663+21C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.615+21C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.539+21C>T
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.681+21C>T
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19773
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7866
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6006
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ

19-42600216-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600216
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600216
    reference: chr 19
allele count: 1
allele frequency: 9.224071136036601e-6
allele num: 108412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.663+18A>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*424+18A>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.615+18A>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.681+18A>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.539+18A>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.669+18A>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.663+18A>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.663+18A>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.643+18A>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.498+18A>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.615+18A>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.615+18A>C
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  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: 21487
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 1.75e1
  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: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5822
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

19-42600218-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600218
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600218
    reference: chr 19
allele count: 1
allele frequency: 9.19320438331985e-6
allele num: 108776
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.615+16G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.615+16G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.663+16G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.663+16G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.539+16G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.643+16G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*424+16G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.669+16G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.663+16G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.498+16G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.681+16G>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.615+16G>C
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9707
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  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 quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

19-42600219-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600219
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600219
    reference: chr 19
allele count: 5
allele frequency: 4.579341673840968e-5
allele num: 109186
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.643+15T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.663+15T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.663+15T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*424+15T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.498+15T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.539+15T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.681+15T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.615+15T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.615+15T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.669+15T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.663+15T>C
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.615+15T>C
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5842
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12983
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23098
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

19-42600225-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600225
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600225
    reference: chr 19
allele count: 6
allele frequency: 5.429569435143793e-5
allele num: 110506
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*424+9G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.498+9G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.663+9G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.663+9G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.643+9G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.615+9G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.663+9G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.681+9G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.615+9G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.539+9G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.669+9G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.615+9G>A
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5052
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13672
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8151
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP

19-42600237-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600237
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600237
    reference: chr 19
allele count: 1
allele frequency: 8.818031110013756e-6
allele num: 113404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.666G>A
  hgvsp: ENST00000560804.2:c.666G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.612G>A
  hgvsp: ENST00000529067.1:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.660G>A
  hgvsp: ENST00000529952.1:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.495G>A
  hgvsp: ENST00000560558.1:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.640G>A
  hgvsp: ENST00000528894.4:c.640G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.536G>A
  hgvsp: ENST00000526831.1:c.536G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.660G>A
  hgvsp: ENST00000342301.4:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.660G>A
  hgvsp: ENST00000526816.2:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.612G>A
  hgvsp: ENST00000533720.1:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.678G>A
  hgvsp: ENST00000560398.1:c.678G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*421G>A
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.612G>A
  hgvsp: ENST00000389341.5:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2567
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29992
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5166
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr220Thr
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

19-42600271-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42600271
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 42600271
    reference: chr 19
allele count: 1
allele frequency: 8.520064752492119e-6
allele num: 117370
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000475664
  ensembl transcript: ENST00000528894
  gene symbol: POU2F2
  hgvsc: ENST00000528894.4:c.606C>G
  hgvsp: ENSP00000475664.1:p.Thr203Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000339369
  ensembl transcript: ENST00000342301
  gene symbol: POU2F2
  hgvsc: ENST00000342301.4:c.626C>G
  hgvsp: ENSP00000339369.4:p.Thr209Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000452930
  ensembl transcript: ENST00000560804
  gene symbol: POU2F2
  hgvsc: ENST00000560804.2:c.632C>G
  hgvsp: ENSP00000452930.2:p.Thr211Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000454179
  ensembl transcript: ENST00000560558
  gene symbol: POU2F2
  hgvsc: ENST00000560558.1:c.461C>G
  hgvsp: ENSP00000454179.1:p.Thr154Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000431603
  ensembl transcript: ENST00000526816
  gene symbol: POU2F2
  hgvsc: ENST00000526816.2:c.626C>G
  hgvsp: ENSP00000431603.3:p.Thr209Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000476062
  ensembl transcript: ENST00000526831
  gene symbol: POU2F2
  hgvsc: ENST00000526831.1:c.502C>G
  hgvsp: ENSP00000476062.1:p.Thr168Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436100
  ensembl transcript: ENST00000534559
  gene symbol: POU2F2
  hgvsc: ENST00000534559.1:c.*387C>G
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000436988
  ensembl transcript: ENST00000529952
  gene symbol: POU2F2
  hgvsc: ENST00000529952.1:c.626C>G
  hgvsp: ENSP00000436988.1:p.Thr209Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000453255
  ensembl transcript: ENST00000560398
  gene symbol: POU2F2
  hgvsc: ENST00000560398.1:c.644C>G
  hgvsp: ENSP00000453255.1:p.Thr215Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000373992
  ensembl transcript: ENST00000389341
  gene symbol: POU2F2
  hgvsc: ENST00000389341.5:c.578C>G
  hgvsp: ENSP00000373992.3:p.Thr193Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437224
  ensembl transcript: ENST00000529067
  gene symbol: POU2F2
  hgvsc: ENST00000529067.1:c.578C>G
  hgvsp: ENSP00000437224.1:p.Thr193Ser
  variant of: http://identifiers.org/hgnc/9213
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000028277
  ensembl protein: ENSP00000437221
  ensembl transcript: ENST00000533720
  gene symbol: POU2F2
  hgvsc: ENST00000533720.1:c.578C>G
  hgvsp: ENSP00000437221.1:p.Thr193Ser
  variant of: http://identifiers.org/hgnc/9213
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 33519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr209Ser
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 2524
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 764
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43059
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 620
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1334
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 711
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9718
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.08794466403162e-5
allele num: 64768
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 1.3113e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.98e0

MQRankSum
type: SiteQuality
SIO_000300: -1.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.13e1

DP
type: SiteQuality
SIO_000300: 1.430587e6

VQSLOD
type: SiteQuality
SIO_000300: -1.683e0

GenotypeQuality
all individuals: 178
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 386
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2660
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 621
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 818
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43714
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6113
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 76
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1690
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1369
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.541782300339192e-5
allele num: 64860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.31e0

DP
type: SiteQuality
SIO_000300: 1.431554e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.102e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 1.7e1

FS
type: SiteQuality
SIO_000300: 3.793e0

VQSLOD
type: SiteQuality
SIO_000300: -9.638e-1

GenotypeQuality
all individuals: 2621
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 651
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6114
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 614
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43339
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1378
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.541402059313151e-5
allele num: 64876
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.431966e6

MQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.627e0

VQSLOD
type: SiteQuality
SIO_000300: -6.127e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

QD
type: SiteQuality
SIO_000300: 1.767e1

GenotypeQuality
all individuals: 180
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1684
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43339
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6114
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1378
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2621
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 468
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.541402059313151e-5
allele num: 64876
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.127e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.57e-1

FS
type: SiteQuality
SIO_000300: 7.627e0

MQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

QD
type: SiteQuality
SIO_000300: 1.767e1

DP
type: SiteQuality
SIO_000300: 1.431966e6

GenotypeQuality
all individuals: 1391
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 9.75e1
variant carriers: 92

GenotypeQuality
all individuals: 106
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42448
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 734
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 708
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1702
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6047
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 9
allele frequency: 7.900280898876404e-4
allele num: 11392
num of homozygotes: 0

East Asian
type: Population
allele count: 83
allele frequency: 9.75093984962406e-3
allele num: 8512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.15473441108545e-3
allele num: 866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6368
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64788
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.48e-1

QD
type: SiteQuality
SIO_000300: 1.267e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.15e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

DP
type: SiteQuality
SIO_000300: 1.437273e6

GenotypeQuality
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6047
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 188
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2548
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1391
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 106
bin: 1.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6368
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.543495709081929e-5
allele num: 64788
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.48e-1

QD
type: SiteQuality
SIO_000300: 1.267e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.15e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.46e-1

DP
type: SiteQuality
SIO_000300: 1.437273e6

GenotypeQuality
all individuals: 282
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42078
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2496
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 873
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6080
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 707
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1395
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1723
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 740
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 4
allele frequency: 4.125412541254125e-4
allele num: 9696
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11396
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6364
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64788
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

QD
type: SiteQuality
SIO_000300: 1.104e1

DP
type: SiteQuality
SIO_000300: 1.436469e6

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

MQ
type: SiteQuality
SIO_000300: 4.931e1

FS
type: SiteQuality
SIO_000300: 3.975e0

MQRankSum
type: SiteQuality
SIO_000300: -5.103e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.316e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

GenotypeQuality
all individuals: 1720
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2495
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 857
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 69
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1381
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6132
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43002
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.54435384235236e-5
allele num: 64752
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6384
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.353494939985879e-4
allele num: 8498
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.2928e1

MQRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.580000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.24e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.165e0

DP
type: SiteQuality
SIO_000300: 1.444482e6

QD
type: SiteQuality
SIO_000300: 2.858e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

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

GenotypeQuality
all individuals: 43239
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1770
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1413
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 800
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2471
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 447
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 654
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6238
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.077549532028686e-5
allele num: 16454
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9728
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64892
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6400
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.798e1

FS
type: SiteQuality
SIO_000300: 1.524e0

DP
type: SiteQuality
SIO_000300: 1.444631e6

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.218e0

MQRankSum
type: SiteQuality
SIO_000300: -3.419e0

MQ
type: SiteQuality
SIO_000300: 5.177e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.42e-1

GenotypeQuality
all individuals: 658
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2471
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43239
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 291
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1770
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 266
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 800
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1413
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 4
allele frequency: 4.111842105263158e-4
allele num: 9728
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64892
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.177e1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.218e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

DP
type: SiteQuality
SIO_000300: 1.444631e6

QD
type: SiteQuality
SIO_000300: 1.798e1

MQRankSum
type: SiteQuality
SIO_000300: -3.419e0

FS
type: SiteQuality
SIO_000300: 1.524e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

GenotypeQuality
all individuals: 96
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1427
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 634
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1772
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6250
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2469
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11396
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6406
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.215362177929023e-4
allele num: 16456
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9730
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64902
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.97e-1

DP
type: SiteQuality
SIO_000300: 1.445244e6

MQRankSum
type: SiteQuality
SIO_000300: 8.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.18e-1

FS
type: SiteQuality
SIO_000300: 7.079e0

QD
type: SiteQuality
SIO_000300: 1.35e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.321e0

GenotypeQuality
all individuals: 726
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42349
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1428
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 862
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variant carriers: 0

GenotypeQuality
all individuals: 6238
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
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variant carriers: 0

GenotypeQuality
all individuals: 345
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variant carriers: 0

GenotypeQuality
all individuals: 2067
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 8.75e1
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GenotypeQuality
all individuals: 267
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 632
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64884
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.778089887640449e-5
allele num: 11392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.067e0

VQSLOD
type: SiteQuality
SIO_000300: 8.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.457283e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.45e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.501e0

QD
type: SiteQuality
SIO_000300: 1.087e1

GenotypeQuality
all individuals: 149
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1761
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6281
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 8.25e1
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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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
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: 9698
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.540642139643804e-5
allele num: 64908
num of homozygotes: 0

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

Other
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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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num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.793527963418924e-5
allele num: 11372
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6464
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South Asian
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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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BaseQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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FS
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MQRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8476
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.542543345468008e-5
allele num: 64828
num of homozygotes: 0

Other
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num of homozygotes: 0

DP
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QD
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 1.123595505617978e-3
allele num: 890
num of homozygotes: 0

South Asian
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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
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 24
allele frequency: 3.679288670856968e-4
allele num: 65230
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.649999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.979e1

VQSLOD
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.491146e6

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 2
allele frequency: 2.35626767200754e-4
allele num: 8488
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65392
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.07e1

FS
type: SiteQuality
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VQSLOD
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DP
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ClippingRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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SIO_000300: -8.0e-4

MQRankSum
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ReadPosRankSum
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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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European (Finnish)
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allele frequency: 0.0e0
allele num: 6544
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Latino
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allele frequency: 0.0e0
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African
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Other
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65564
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FS
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ClippingRankSum
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QD
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MQ
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 1.001803245842517e-4
allele num: 9982
num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

South Asian
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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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BaseQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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MQ
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MQRankSum
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ClippingRankSum
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DP
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QD
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ReadPosRankSum
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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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East Asian
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South Asian
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European (Non-Finnish)
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African
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European (Finnish)
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Latino
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Other
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FS
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VQSLOD
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MQRankSum
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DP
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InbreedingCoeff
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BaseQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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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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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
all individuals: 314
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 86
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509115054931788e-5
allele num: 66264
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e0

VQSLOD
type: SiteQuality
SIO_000300: 6.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.99e0

QD
type: SiteQuality
SIO_000300: 1.42e1

MQRankSum
type: SiteQuality
SIO_000300: 5.38e-1

FS
type: SiteQuality
SIO_000300: 1.265e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e0

DP
type: SiteQuality
SIO_000300: 1.529291e6

GenotypeQuality
all individuals: 208
bin: 8.75e1
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
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.016409266409266e-5
allele num: 66304
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-1

QD
type: SiteQuality
SIO_000300: 1.084e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.59e-1

FS
type: SiteQuality
SIO_000300: 8.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.3e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.53044e6

MQRankSum
type: SiteQuality
SIO_000300: 4.34e-1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 210
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GenotypeQuality
all individuals: 715
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506477854775535e-5
allele num: 66380
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.77e-1

QD
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SIO_000300: 9.800000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

DP
type: SiteQuality
SIO_000300: 1.532489e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.357e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-1

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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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
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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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 317
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506477854775535e-5
allele num: 66380
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.800000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.357e0

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

DP
type: SiteQuality
SIO_000300: 1.532489e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.77e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: 3.54e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 13
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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
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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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GenotypeQuality
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GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 9.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.012325266796934e-5
allele num: 66530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.96e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

QD
type: SiteQuality
SIO_000300: 1.245e1

FS
type: SiteQuality
SIO_000300: 2.235e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.28e-1

MQRankSum
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SIO_000300: 2.48e-1

BaseQRankSum
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SIO_000300: -2.224e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.53549e6

GenotypeDepth
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 15
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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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variant carriers: 2

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: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66548
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.933488012374323e-4
allele num: 10344
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.604e-1

ClippingRankSum
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BaseQRankSum
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FS
type: SiteQuality
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DP
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InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.957e1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

QD
type: SiteQuality
SIO_000300: 1.07e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.32e0

GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 711
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GenotypeQuality
all individuals: 159
bin: 2.25e1
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: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
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: 1
allele frequency: 1.160362032954282e-4
allele num: 8618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66562
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.43e0

ReadPosRankSum
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QD
type: SiteQuality
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ClippingRankSum
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DP
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MQRankSum
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VQSLOD
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MQ
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SIO_000300: 5.943e1

InbreedingCoeff
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SIO_000300: 3.3e-3

BaseQRankSum
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GenotypeDepth
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variant carriers: 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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GenotypeQuality
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GenotypeQuality
all individuals: 188
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GenotypeQuality
all individuals: 318
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variant carriers: 2

GenotypeQuality
all individuals: 48617
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004627125773691e-5
allele num: 66564
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

VQSLOD
type: SiteQuality
SIO_000300: 7.75e-1

FS
type: SiteQuality
SIO_000300: 6.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.7e-2

DP
type: SiteQuality
SIO_000300: 1.536363e6

MQ
type: SiteQuality
SIO_000300: 5.978e1

QD
type: SiteQuality
SIO_000300: 1.48e1

GenotypeDepth
all individuals: 1058
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50195253829979e-5
allele num: 66580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.536592e6

VQSLOD
type: SiteQuality
SIO_000300: -2.21e0

MQRankSum
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SIO_000300: 1.31e0

ReadPosRankSum
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SIO_000300: 6.75e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

BaseQRankSum
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SIO_000300: -2.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

QD
type: SiteQuality
SIO_000300: 4.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e0

FS
type: SiteQuality
SIO_000300: 1.433e0

GenotypeDepth
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bin: 8.25e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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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variant carriers: 7

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.239854633555421e-4
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
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: -3.483e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 5.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-3

QD
type: SiteQuality
SIO_000300: 1.216e1

MQRankSum
type: SiteQuality
SIO_000300: -3.1e-1

DP
type: SiteQuality
SIO_000300: 1.538041e6

MQ
type: SiteQuality
SIO_000300: 5.944e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.0e-1

GenotypeDepth
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bin: 1.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 1
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variant carriers: 1

GenotypeDepth
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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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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000750187546887e-5
allele num: 66650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.538349e6

MQRankSum
type: SiteQuality
SIO_000300: 1.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.85e-1

QD
type: SiteQuality
SIO_000300: 1.477e1

VQSLOD
type: SiteQuality
SIO_000300: -7.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

FS
type: SiteQuality
SIO_000300: 3.551e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeDepth
all individuals: 64
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
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variant carriers: 1

GenotypeDepth
all individuals: 1
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variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
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variant carriers: 0

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

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 328
bin: 9.75e1
variant carriers: 11

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

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

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.650016500165002e-4
allele num: 66666
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
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: 10374
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.945e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

QD
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SIO_000300: 1.324e1

ClippingRankSum
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SIO_000300: 4.14e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.3e-2

DP
type: SiteQuality
SIO_000300: 1.539406e6

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 27
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
all individuals: 15
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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: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1854
bin: 7.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.633911368015414e-5
allele num: 10380
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -4.66e-1

MQRankSum
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SIO_000300: 1.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.811e0

VQSLOD
type: SiteQuality
SIO_000300: 2.58e0

ReadPosRankSum
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SIO_000300: 5.22e-1

QD
type: SiteQuality
SIO_000300: 1.815e1

DP
type: SiteQuality
SIO_000300: 1.538871e6

GenotypeDepth
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variant carriers: 9

GenotypeDepth
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variant carriers: 11

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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: 190

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: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 3
allele frequency: 2.887391722810395e-4
allele num: 10390
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.774706288873532e-4
allele num: 11576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 174
allele frequency: 2.609321576390139e-3
allele num: 66684
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.94e-1

FS
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -1.5e-3

VQSLOD
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ReadPosRankSum
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ClippingRankSum
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.208e1

MQ
type: SiteQuality
SIO_000300: 5.945e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
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European (Non-Finnish)
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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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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.916e1

ClippingRankSum
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QD
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FS
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MQRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

European (Finnish)
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allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

Other
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East Asian
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allele frequency: 0.0e0
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Latino
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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MQ
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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QD
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FS
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DP
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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SIO_000300: -1.973e0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 42

East Asian
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num of homozygotes: 0

South Asian
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allele frequency: 2.394694829915265e-3
allele num: 16286
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European (Non-Finnish)
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allele frequency: 1.502810255177181e-5
allele num: 66542
num of homozygotes: 0

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

Latino
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ClippingRankSum
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SIO_000300: -1.1e-1

VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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DP
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BaseQRankSum
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MQ
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FS
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MQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 6.244536030972898e-5
allele num: 16014
num of homozygotes: 0

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

Other
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East Asian
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allele frequency: 0.0e0
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Latino
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African
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European (Finnish)
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ReadPosRankSum
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QD
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FS
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 1.162520344106022e-4
allele num: 8602
num of homozygotes: 0

Other
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European (Finnish)
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European (Non-Finnish)
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Latino
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African
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South Asian
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QD
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FS
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ClippingRankSum
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BaseQRankSum
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DP
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MQ
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ReadPosRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Non-Finnish)
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allele num: 65882
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African
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Latino
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European (Finnish)
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Other
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ReadPosRankSum
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FS
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QD
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MQRankSum
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ClippingRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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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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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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European (Finnish)
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Other
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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InbreedingCoeff
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MQ
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QD
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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FS
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MQRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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African
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Other
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num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.606429192006951e-4
allele num: 11510
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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FS
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DP
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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QD
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MQ
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ClippingRankSum
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SIO_000300: -2.67e-1

GenotypeDepth
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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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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

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

European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Latino
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allele num: 11510
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African
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Other
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ClippingRankSum
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InbreedingCoeff
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FS
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DP
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MQRankSum
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MQ
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.526717557251908e-5
allele num: 65500
num of homozygotes: 0

African
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South Asian
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Latino
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Other
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
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DP
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FS
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InbreedingCoeff
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MQ
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QD
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: 5.87e-1

GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.97667523225934e-4
allele num: 10118
num of homozygotes: 0

Other
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South Asian
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allele count: 0
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

European (Non-Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
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SIO_000300: 1.8e-3

VQSLOD
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FS
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ClippingRankSum
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MQRankSum
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MQ
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BaseQRankSum
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DP
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QD
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ReadPosRankSum
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SIO_000300: 1.52e0

GenotypeDepth
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variant carriers: 3

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

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

African
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num of homozygotes: 0

European (Non-Finnish)
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South Asian
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East Asian
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InbreedingCoeff
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MQ
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ClippingRankSum
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VQSLOD
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MQRankSum
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DP
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FS
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BaseQRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 4.006410256410256e-4
allele num: 14976
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.712319219376198e-5
allele num: 11478
num of homozygotes: 0

European (Finnish)
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European (Non-Finnish)
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East Asian
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Other
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MQRankSum
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ReadPosRankSum
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QD
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MQ
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DP
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FS
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

African
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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Other
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DP
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FS
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BaseQRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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QD
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 46
allele frequency: 4.594486616060727e-3
allele num: 10012
num of homozygotes: 0

Other
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East Asian
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allele frequency: 0.0e0
allele num: 8514
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
allele num: 14740
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European (Non-Finnish)
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Latino
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ReadPosRankSum
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SIO_000300: 3.42e-1

InbreedingCoeff
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QD
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VQSLOD
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MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

FS
type: SiteQuality
SIO_000300: 9.350000000000001e-1

BaseQRankSum
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SIO_000300: -2.712e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-2

DP
type: SiteQuality
SIO_000300: 1.438478e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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variant carriers: 3

GenotypeQuality
all individuals: 313
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64780
num of homozygotes: 0

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

Latino
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allele count: 3
allele frequency: 2.632502632502633e-4
allele num: 11396
num of homozygotes: 0

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

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

MQRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQ
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DP
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FS
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ClippingRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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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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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 (Non-Finnish)
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allele frequency: 0.0e0
allele num: 64060
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele frequency: 3.564638783269962e-4
allele num: 8416
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9814
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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FS
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SIO_000300: 0.0e0

BaseQRankSum
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DP
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MQ
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VQSLOD
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MQRankSum
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QD
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InbreedingCoeff
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SIO_000300: -7.0e-4

ClippingRankSum
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SIO_000300: -5.85e-1

ReadPosRankSum
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SIO_000300: 3.02e-1

GenotypeDepth
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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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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: 2

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

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

South Asian
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allele frequency: 1.380834023750345e-4
allele num: 14484
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63680
num of homozygotes: 0

Other
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.49e-1

MQ
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FS
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VQSLOD
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DP
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InbreedingCoeff
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SIO_000300: 1.6e-3

MQRankSum
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QD
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BaseQRankSum
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SIO_000300: -6.41e-1

ClippingRankSum
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SIO_000300: -5.1e-1

GenotypeDepth
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GenotypeQuality
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variant carriers: 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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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.741134079271762e-5
allele num: 63276
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6394
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

East Asian
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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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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
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SIO_000300: 1.357569e6

ReadPosRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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ClippingRankSum
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QD
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele num: 842
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: 1.05241001894338e-4
allele num: 9502
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11112
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62464
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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QD
type: SiteQuality
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FS
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MQ
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

African
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allele frequency: 1.095770326539557e-4
allele num: 9126
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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South Asian
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Latino
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QD
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MQ
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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FS
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MQRankSum
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DP
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8872
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9894
num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 57212
num of homozygotes: 0

European (Finnish)
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Other
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South Asian
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FS
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MQRankSum
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MQ
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VQSLOD
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QD
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DP
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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DP
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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BaseQRankSum
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QD
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FS
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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East Asian
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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FS
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InbreedingCoeff
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VQSLOD
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MQRankSum
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MQ
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BaseQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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QD
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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African
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Other
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ReadPosRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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MQRankSum
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VQSLOD
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MQ
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QD
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ClippingRankSum
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DP
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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allele num: 8994
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Latino
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European (Finnish)
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Other
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European (Non-Finnish)
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South Asian
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VQSLOD
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ClippingRankSum
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MQ
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DP
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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FS
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QD
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

African
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European (Non-Finnish)
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Latino
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East Asian
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South Asian
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Other
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MQRankSum
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VQSLOD
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MQ
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DP
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FS
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BaseQRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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African
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European (Finnish)
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South Asian
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European (Non-Finnish)
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East Asian
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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MQRankSum
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VQSLOD
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FS
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QD
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ClippingRankSum
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MQ
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GenotypeDepth
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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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African
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European (Finnish)
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East Asian
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European (Non-Finnish)
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South Asian
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Latino
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DP
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ReadPosRankSum
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QD
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MQ
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MQRankSum
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FS
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VQSLOD
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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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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3631
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1156
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9152
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.676108745935436e-5
allele num: 59662
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5388
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7688
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15790
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

DP
type: SiteQuality
SIO_000300: 1.219044e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.6e-2

MQ
type: SiteQuality
SIO_000300: 5.883e1

QD
type: SiteQuality
SIO_000300: 1.402e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.5e-1

GenotypeDepth
all individuals: 108
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 990
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32248
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2706
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3697
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.346688034188034e-5
allele num: 59904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5414
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15804
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.488e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.702e0

DP
type: SiteQuality
SIO_000300: 1.226746e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.64e-1

QD
type: SiteQuality
SIO_000300: 1.26e1

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

GenotypeDepth
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bin: 3.25e1
variant carriers: 2

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 675
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3972
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5460
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.562057754828839e-5
allele num: 10458
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.222493887530562e-3
allele num: 818
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.646524187440313e-5
allele num: 60734
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7858
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9322
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.892028254288597e-4
allele num: 15856
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.83e-1

FS
type: SiteQuality
SIO_000300: 2.467e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.224e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

QD
type: SiteQuality
SIO_000300: 1.025e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.61e-1

DP
type: SiteQuality
SIO_000300: 1.25778e6

GenotypeDepth
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bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
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variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15193
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5828
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1924
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4453
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variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41076
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9508
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8176
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15948
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10766
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.598158920923096e-5
allele num: 62572
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.202e0

VQSLOD
type: SiteQuality
SIO_000300: 2.65e-1

DP
type: SiteQuality
SIO_000300: 1.328684e6

FS
type: SiteQuality
SIO_000300: 4.246e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

QD
type: SiteQuality
SIO_000300: 9.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.27e0