19-9525392-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9525392
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9525392
    reference: chr 19
allele count: 1
allele frequency: 8.845956513277781e-6
allele num: 113046
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.209G>A
  hgvsp: ENSP00000467315.1:p.Gly70Glu
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.209G>A
  hgvsp: ENSP00000466714.1:p.Gly70Glu
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.209G>A
  hgvsp: ENSP00000354680.2:p.Gly70Glu
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.209G>A
  hgvsp: ENSP00000355047.1:p.Gly70Glu
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.209G>A
  hgvsp: ENSP00000467151.1:p.Gly70Glu
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.209G>A
  hgvsp: ENSP00000467403.1:p.Gly70Glu
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.209G>A
  hgvsp: ENSP00000467923.1:p.Gly70Glu
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.209G>A
  hgvsp: ENSP00000468491.1:p.Gly70Glu
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4866
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1372
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9519
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3489
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly70Glu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

19-9525399-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9525399
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9525399
    reference: chr 19
allele count: 1
allele frequency: 8.918060856847287e-6
allele num: 112132
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.205-3C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.205-3C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.205-3C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.205-3C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.205-3C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.205-3C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.205-3C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.205-3C>T
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2682
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3875
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4715
  bin: 7.75e1
  variant carriers: 0
hgvs: c.205-3C>T
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

19-9525419-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9525419
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9525419
    reference: chr 19
allele count: 7
allele frequency: 6.316321374431532e-5
allele num: 110824
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.205-23A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.205-23A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.205-23A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.205-23A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.205-23A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.205-23A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.205-23A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.205-23A>G
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2682
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10768
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9125
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1890
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3854
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4700
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

19-9525424-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9525424
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9525424
    reference: chr 19
allele count: 7
allele frequency: 6.332320162107397e-5
allele num: 110544
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.205-28T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.205-28T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.205-28T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.205-28T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.205-28T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.205-28T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.205-28T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.205-28T>C
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8784
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9652
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10740
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3130
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3489
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4695
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

19-9525427-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9525427
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9525427
    reference: chr 19
allele count: 3
allele frequency: 2.718918233065671e-5
allele num: 110338
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.205-31C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.205-31C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.205-31C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.205-31C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.205-31C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.205-31C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.205-31C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.205-31C>G
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9650
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3130
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5524
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3488
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3843
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

19-9525430-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9525430
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9525430
    reference: chr 19
allele count: 4
allele frequency: 3.628249551004118e-5
allele num: 110246
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.205-34G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.205-34G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.205-34G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.205-34G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.205-34G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.205-34G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.205-34G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.205-34G>A
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9652
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4691
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5524
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

19-9525431-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9525431
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9525431
    reference: chr 19
allele count: 8
allele frequency: 7.264010460175062e-5
allele num: 110132
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.205-35C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.205-35C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.205-35C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.205-35C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.205-35C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.205-35C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.205-35C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.205-35C>T
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8574
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9651
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3482
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2823
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5486
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4357
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 988
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4688
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

19-9525436-AGATT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9525436
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9525432
    reference: chr 19
allele count: 1
allele frequency: 9.087109027134107e-6
allele num: 110046
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.205-44_205-41delAATC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.205-44_205-41delAATC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.205-44_205-41delAATC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.205-44_205-41delAATC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.205-44_205-41delAATC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.205-44_205-41delAATC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.205-44_205-41delAATC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.205-44_205-41delAATC
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8186
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3040
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2827
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4683
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: AGATT
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

19-9525438-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9525438
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9525438
    reference: chr 19
allele count: 8
allele frequency: 7.272727272727273e-5
allele num: 110000
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.205-42T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.205-42T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.205-42T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.205-42T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.205-42T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.205-42T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.205-42T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.205-42T>C
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7315
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8353
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3835
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4683
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8077
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

19-9525439-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9525439
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9525439
    reference: chr 19
allele count: 1
allele frequency: 9.091239681442962e-6
allele num: 109996
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.205-43A>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.205-43A>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.205-43A>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.205-43A>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.205-43A>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.205-43A>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.205-43A>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.205-43A>T
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7314
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3829
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4361
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20197
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2824
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4685
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

19-9525439-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9525439
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9525439
    reference: chr 19
allele count: 11
allele frequency: 1.000036364958726e-4
allele num: 109996
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.205-43A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.205-43A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.205-43A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.205-43A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.205-43A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.205-43A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.205-43A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.205-43A>G
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8360
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7314
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4685
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4361
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3486
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8136
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

19-9526282-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526282
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526282
    reference: chr 19
allele count: 1
allele frequency: 8.299443937256203e-6
allele num: 120490
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.204+48G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.204+48G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.204+48G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.204+48G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.204+48G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.204+48G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.204+48G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.204+48G>A
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10325
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15080
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4701
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12319
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2154
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2623
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

19-9526283-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526283
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526283
    reference: chr 19
allele count: 1
allele frequency: 8.285416010737898e-6
allele num: 120694
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.204+47T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.204+47T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.204+47T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.204+47T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.204+47T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.204+47T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.204+47T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.204+47T>A
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15124
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10343
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4005
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1500
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1986
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP

19-9526284-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526284
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526284
    reference: chr 19
allele count: 6
allele frequency: 4.971084856418499e-5
allele num: 120698
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.204+46T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.204+46T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.204+46T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.204+46T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.204+46T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.204+46T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.204+46T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.204+46T>C
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15179
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13048
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10353
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3569
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2632
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16597
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 890
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7432
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

19-9526288-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526288
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526288
    reference: chr 19
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.204+42A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.204+42A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.204+42A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.204+42A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.204+42A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.204+42A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.204+42A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.204+42A>G
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14542
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7550
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

19-9526293-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526293
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526293
    reference: chr 19
allele count: 1
allele frequency: 8.279105194310599e-6
allele num: 120786
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.204+37T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.204+37T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.204+37T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.204+37T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.204+37T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.204+37T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.204+37T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.204+37T>A
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5903
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15716
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5084
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20687
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-9526294-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526294
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526294
    reference: chr 19
allele count: 18
allele frequency: 1.48964695367198e-4
allele num: 120834
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.204+36T>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.204+36T>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.204+36T>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.204+36T>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.204+36T>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.204+36T>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.204+36T>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.204+36T>G
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16147
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5904
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15792
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10624
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12105
  bin: 9.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3625
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum

19-9526299-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526299
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526300
    reference: chr 19
allele count: 1
allele frequency: 8.268152729317216e-6
allele num: 120946
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.204+30dupT
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.204+30dupT
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.204+30dupT
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.204+30dupT
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.204+30dupT
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.204+30dupT
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.204+30dupT
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.204+30dupT
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16641
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21870
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5108
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2661
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4038
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-9526303-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526303
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526303
    reference: chr 19
allele count: 1
allele frequency: 8.260366760284156e-6
allele num: 121060
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.204+27T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.204+27T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.204+27T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.204+27T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.204+27T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.204+27T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.204+27T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.204+27T>A
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10736
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22421
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2662
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

19-9526307-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526307
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526307
    reference: chr 19
allele count: 2
allele frequency: 1.650628063978344e-5
allele num: 121166
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.204+23T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.204+23T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.204+23T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.204+23T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.204+23T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.204+23T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.204+23T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.204+23T>C
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10762
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22791
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1987
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4053
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3680
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

19-9526308-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526308
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526308
    reference: chr 19
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.204+22C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.204+22C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.204+22C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.204+22C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.204+22C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.204+22C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.204+22C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.204+22C>G
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5931
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7803
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2663
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum

19-9526311-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526311
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526311
    reference: chr 19
allele count: 4
allele frequency: 3.299132328197684e-5
allele num: 121244
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.204+19C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.204+19C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.204+19C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.204+19C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.204+19C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.204+19C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.204+19C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.204+19C>T
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1989
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5141
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3673
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

19-9526314-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526314
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526314
    reference: chr 19
allele count: 64
allele frequency: 5.277044854881266e-4
allele num: 121280
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.204+16A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.204+16A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.204+16A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.204+16A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.204+16A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.204+16A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.204+16A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.204+16A>G
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 17193
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10794
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5930
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 4.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23015
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

19-9526318-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526318
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526318
    reference: chr 19
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.204+12A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.204+12A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.204+12A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.204+12A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.204+12A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.204+12A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.204+12A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.204+12A>G
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5937
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23095
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7844
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

19-9526332-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526332
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526332
    reference: chr 19
allele count: 3
allele frequency: 2.471576866040534e-5
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.202A>T
  hgvsp: ENSP00000467923.1:p.Met68Leu
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.202A>T
  hgvsp: ENSP00000466714.1:p.Met68Leu
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.202A>T
  hgvsp: ENSP00000467403.1:p.Met68Leu
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.202A>T
  hgvsp: ENSP00000467315.1:p.Met68Leu
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.202A>T
  hgvsp: ENSP00000467151.1:p.Met68Leu
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.202A>T
  hgvsp: ENSP00000354680.2:p.Met68Leu
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.202A>T
  hgvsp: ENSP00000355047.1:p.Met68Leu
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.202A>T
  hgvsp: ENSP00000468491.1:p.Met68Leu
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16598
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23179
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Met68Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/19-9526343-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526343
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526343
    reference: chr 19
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.191G>T
  hgvsp: ENSP00000354680.2:p.Ser64Ile
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.191G>T
  hgvsp: ENSP00000466714.1:p.Ser64Ile
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.191G>T
  hgvsp: ENSP00000467315.1:p.Ser64Ile
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.191G>T
  hgvsp: ENSP00000467403.1:p.Ser64Ile
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.191G>T
  hgvsp: ENSP00000467923.1:p.Ser64Ile
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.191G>T
  hgvsp: ENSP00000468491.1:p.Ser64Ile
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.191G>T
  hgvsp: ENSP00000467151.1:p.Ser64Ile
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.191G>T
  hgvsp: ENSP00000355047.1:p.Ser64Ile
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12088
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2665
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3687
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser64Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-9526350-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526350
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526350
    reference: chr 19
allele count: 4
allele frequency: 3.294838635277837e-5
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.184A>G
  hgvsp: ENSP00000355047.1:p.Thr62Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.184A>G
  hgvsp: ENSP00000354680.2:p.Thr62Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.184A>G
  hgvsp: ENSP00000466714.1:p.Thr62Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.184A>G
  hgvsp: ENSP00000468491.1:p.Thr62Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.184A>G
  hgvsp: ENSP00000467151.1:p.Thr62Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.184A>G
  hgvsp: ENSP00000467315.1:p.Thr62Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.184A>G
  hgvsp: ENSP00000467403.1:p.Thr62Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.184A>G
  hgvsp: ENSP00000467923.1:p.Thr62Ala
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17185
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2666
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3688
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr62Ala
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

19-9526351-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526351
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526351
    reference: chr 19
allele count: 2
allele frequency: 1.647446457990115e-5
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.183A>C
  hgvsp: ENST00000361451.2:c.183A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.183A>C
  hgvsp: ENST00000361151.1:c.183A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.183A>C
  hgvsp: ENST00000591213.1:c.183A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.183A>C
  hgvsp: ENST00000592904.1:c.183A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.183A>C
  hgvsp: ENST00000592292.1:c.183A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.183A>C
  hgvsp: ENST00000588933.1:c.183A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.183A>C
  hgvsp: ENST00000590306.1:c.183A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.183A>C
  hgvsp: ENST00000588221.1:c.183A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7853
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro61Pro
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-9526359-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526359
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526360
    reference: chr 19
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.174_175insT
  hgvsp: ENSP00000354680.2:p.Gly59TrpfsTer21
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.174_175insT
  hgvsp: ENSP00000355047.1:p.Gly59TrpfsTer21
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.174_175insT
  hgvsp: ENSP00000467923.1:p.Gly59TrpfsTer?
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.174_175insT
  hgvsp: ENSP00000467403.1:p.Gly59TrpfsTer21
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.174_175insT
  hgvsp: ENSP00000467315.1:p.Gly59TrpfsTer21
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.174_175insT
  hgvsp: ENSP00000468491.1:p.Gly59TrpfsTer21
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.174_175insT
  hgvsp: ENSP00000467151.1:p.Gly59TrpfsTer21
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.174_175insT
  hgvsp: ENSP00000466714.1:p.Gly59TrpfsTer21
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16640
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7850
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4058
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12091
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3688
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly59TrpfsTer21
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/19-9526360-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526360
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526360
    reference: chr 19
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.174G>T
  hgvsp: ENSP00000466714.1:p.Leu58Phe
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.174G>T
  hgvsp: ENSP00000467315.1:p.Leu58Phe
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.174G>T
  hgvsp: ENSP00000354680.2:p.Leu58Phe
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.174G>T
  hgvsp: ENSP00000468491.1:p.Leu58Phe
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.174G>T
  hgvsp: ENSP00000467151.1:p.Leu58Phe
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.174G>T
  hgvsp: ENSP00000467923.1:p.Leu58Phe
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.174G>T
  hgvsp: ENSP00000467403.1:p.Leu58Phe
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.174G>T
  hgvsp: ENSP00000355047.1:p.Leu58Phe
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10820
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23196
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7852
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu58Phe
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

19-9526362-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526362
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526362
    reference: chr 19
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.172T>C
  hgvsp: ENST00000592292.1:c.172T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.172T>C
  hgvsp: ENST00000361151.1:c.172T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.172T>C
  hgvsp: ENST00000588933.1:c.172T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.172T>C
  hgvsp: ENST00000592904.1:c.172T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.172T>C
  hgvsp: ENST00000588221.1:c.172T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.172T>C
  hgvsp: ENST00000361451.2:c.172T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.172T>C
  hgvsp: ENST00000590306.1:c.172T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.172T>C
  hgvsp: ENST00000591213.1:c.172T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17173
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23202
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4057
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1990
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu58Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-9526367-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526367
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526367
    reference: chr 19
allele count: 3
allele frequency: 2.471169686985173e-5
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.167A>G
  hgvsp: ENSP00000467923.1:p.Asp56Gly
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.167A>G
  hgvsp: ENSP00000467403.1:p.Asp56Gly
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.167A>G
  hgvsp: ENSP00000466714.1:p.Asp56Gly
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.167A>G
  hgvsp: ENSP00000468491.1:p.Asp56Gly
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.167A>G
  hgvsp: ENSP00000467151.1:p.Asp56Gly
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.167A>G
  hgvsp: ENSP00000467315.1:p.Asp56Gly
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.167A>G
  hgvsp: ENSP00000355047.1:p.Asp56Gly
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.167A>G
  hgvsp: ENSP00000354680.2:p.Asp56Gly
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17170
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5942
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3688
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1990
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp56Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

19-9526374-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526374
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526374
    reference: chr 19
allele count: 45
allele frequency: 3.706815598280038e-4
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.160C>T
  hgvsp: ENSP00000468491.1:p.Gln54Ter
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.160C>T
  hgvsp: ENSP00000355047.1:p.Gln54Ter
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.160C>T
  hgvsp: ENSP00000467403.1:p.Gln54Ter
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.160C>T
  hgvsp: ENSP00000467315.1:p.Gln54Ter
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.160C>T
  hgvsp: ENSP00000354680.2:p.Gln54Ter
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.160C>T
  hgvsp: ENSP00000467923.1:p.Gln54Ter
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.160C>T
  hgvsp: ENSP00000467151.1:p.Gln54Ter
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.160C>T
  hgvsp: ENSP00000466714.1:p.Gln54Ter
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5941
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 9.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4054
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3686
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gln54Ter
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

19-9526379-GCTAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526379
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526375
    reference: chr 19
allele count: 3
allele frequency: 2.471210398853358e-5
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.151_154delTTAG
  hgvsp: ENSP00000355047.1:p.Leu51ProfsTer17
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.151_154delTTAG
  hgvsp: ENSP00000467923.1:p.Leu51ProfsTer17
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.151_154delTTAG
  hgvsp: ENSP00000467151.1:p.Leu51ProfsTer17
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.151_154delTTAG
  hgvsp: ENSP00000467403.1:p.Leu51ProfsTer17
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.151_154delTTAG
  hgvsp: ENSP00000354680.2:p.Leu51ProfsTer17
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.151_154delTTAG
  hgvsp: ENSP00000467315.1:p.Leu51ProfsTer17
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.151_154delTTAG
  hgvsp: ENSP00000466714.1:p.Leu51ProfsTer17
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.151_154delTTAG
  hgvsp: ENSP00000468491.1:p.Leu51ProfsTer17
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7850
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu51ProfsTer17
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: GCTAA
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

19-9526384-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526384
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526384
    reference: chr 19
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.150G>A
  hgvsp: ENST00000361151.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.150G>A
  hgvsp: ENST00000592292.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.150G>A
  hgvsp: ENST00000591213.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.150G>A
  hgvsp: ENST00000588221.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.150G>A
  hgvsp: ENST00000590306.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.150G>A
  hgvsp: ENST00000588933.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.150G>A
  hgvsp: ENST00000361451.2:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.150G>A
  hgvsp: ENST00000592904.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5939
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5145
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1990
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu50Glu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-9526391-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526391
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526391
    reference: chr 19
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.143C>T
  hgvsp: ENSP00000354680.2:p.Thr48Ile
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.143C>T
  hgvsp: ENSP00000467403.1:p.Thr48Ile
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.143C>T
  hgvsp: ENSP00000466714.1:p.Thr48Ile
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.143C>T
  hgvsp: ENSP00000468491.1:p.Thr48Ile
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.143C>T
  hgvsp: ENSP00000355047.1:p.Thr48Ile
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.143C>T
  hgvsp: ENSP00000467151.1:p.Thr48Ile
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.143C>T
  hgvsp: ENSP00000467923.1:p.Thr48Ile
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.143C>T
  hgvsp: ENSP00000467315.1:p.Thr48Ile
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2663
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr48Ile
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum

http://identifiers.org/exac.variant/19-9526397-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526397
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526397
    reference: chr 19
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.137T>G
  hgvsp: ENSP00000354680.2:p.Leu46Arg
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.137T>G
  hgvsp: ENSP00000467923.1:p.Leu46Arg
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.137T>G
  hgvsp: ENSP00000467151.1:p.Leu46Arg
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.137T>G
  hgvsp: ENSP00000468491.1:p.Leu46Arg
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.137T>G
  hgvsp: ENSP00000466714.1:p.Leu46Arg
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.137T>G
  hgvsp: ENSP00000467403.1:p.Leu46Arg
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.137T>G
  hgvsp: ENSP00000355047.1:p.Leu46Arg
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.137T>G
  hgvsp: ENSP00000467315.1:p.Leu46Arg
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16669
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2663
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu46Arg
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

19-9526402-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526402
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526402
    reference: chr 19
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.132G>A
  hgvsp: ENST00000592292.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.132G>A
  hgvsp: ENST00000361151.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.132G>A
  hgvsp: ENST00000591213.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.132G>A
  hgvsp: ENST00000590306.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.132G>A
  hgvsp: ENST00000588221.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.132G>A
  hgvsp: ENST00000588933.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.132G>A
  hgvsp: ENST00000361451.2:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.132G>A
  hgvsp: ENST00000592904.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16673
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12088
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4057
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val44Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

19-9526403-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526403
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526403
    reference: chr 19
allele count: 2
allele frequency: 1.647690761397901e-5
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.131T>C
  hgvsp: ENSP00000354680.2:p.Val44Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.131T>C
  hgvsp: ENSP00000466714.1:p.Val44Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.131T>C
  hgvsp: ENSP00000467151.1:p.Val44Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.131T>C
  hgvsp: ENSP00000355047.1:p.Val44Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.131T>C
  hgvsp: ENSP00000467923.1:p.Val44Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.131T>C
  hgvsp: ENSP00000467403.1:p.Val44Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.131T>C
  hgvsp: ENSP00000467315.1:p.Val44Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.131T>C
  hgvsp: ENSP00000468491.1:p.Val44Ala
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23147
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12087
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val44Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

19-9526418-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526418
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526418
    reference: chr 19
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.116C>G
  hgvsp: ENSP00000467315.1:p.Ala39Gly
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.116C>G
  hgvsp: ENSP00000355047.1:p.Ala39Gly
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.116C>G
  hgvsp: ENSP00000467151.1:p.Ala39Gly
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.116C>G
  hgvsp: ENSP00000468491.1:p.Ala39Gly
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.116C>G
  hgvsp: ENSP00000354680.2:p.Ala39Gly
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.116C>G
  hgvsp: ENSP00000467923.1:p.Ala39Gly
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.116C>G
  hgvsp: ENSP00000467403.1:p.Ala39Gly
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.116C>G
  hgvsp: ENSP00000466714.1:p.Ala39Gly
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16685
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10837
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22839
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala39Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/19-9526422-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526422
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526422
    reference: chr 19
allele count: 24
allele frequency: 1.97912028103508e-4
allele num: 121266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.116-4T>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.116-4T>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.116-4T>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.116-4T>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.116-4T>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.116-4T>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.116-4T>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.116-4T>G
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5936
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10819
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22574
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2659
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1987
  bin: 8.75e1
  variant carriers: 0
hgvs: c.116-4T>G
num of homozygotes: 1
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

19-9526436-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526436
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526436
    reference: chr 19
allele count: 1
allele frequency: 8.260503229856763e-6
allele num: 121058
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.116-18A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.116-18A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.116-18A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.116-18A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.116-18A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.116-18A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.116-18A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.116-18A>G
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16538
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10842
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4046
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2658
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7662
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3656
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5127
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

19-9526465-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526465
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526465
    reference: chr 19
allele count: 5
allele frequency: 4.14765657403567e-5
allele num: 120550
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.116-47G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.116-47G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.116-47G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.116-47G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.116-47G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.116-47G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.116-47G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.116-47G>A
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13948
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13193
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10334
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2526
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 797
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1005
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1482
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3973
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD

19-9526465-CAGAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526465
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526461
    reference: chr 19
allele count: 1
allele frequency: 8.29531314807134e-6
allele num: 120550
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.116-51_116-48delATCT
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.116-51_116-48delATCT
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.116-51_116-48delATCT
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.116-51_116-48delATCT
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.116-51_116-48delATCT
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.116-51_116-48delATCT
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.116-51_116-48delATCT
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.116-51_116-48delATCT
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10334
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1482
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6656
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1005
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13179
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3488
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2645
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: CAGAT
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

19-9526469-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9526469
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9526470
    reference: chr 19
allele count: 1
allele frequency: 8.304268393954492e-6
allele num: 120420
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.116-52dupC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.116-52dupC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.116-52dupC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.116-52dupC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.116-52dupC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.116-52dupC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.116-52dupC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.116-52dupC
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10182
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3988
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3229
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12075
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4965
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2651
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

19-9528467-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528467
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528467
    reference: chr 19
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.115+37T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.115+37T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.115+37T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.115+37T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.115+37T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.115+37T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.115+37T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.115+37T>C
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11233
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51604
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

19-9528471-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528471
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528471
    reference: chr 19
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.115+33A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.115+33A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.115+33A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.115+33A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.115+33A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.115+33A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.115+33A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.115+33A>G
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11233
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4501
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

19-9528473-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528473
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528473
    reference: chr 19
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.115+31A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.115+31A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.115+31A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.115+31A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.115+31A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.115+31A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.115+31A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.115+31A>G
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4501
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11232
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 6.75e1
  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: 4538
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1314
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51605
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1195
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1173
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

19-9528476-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528476
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528476
    reference: chr 19
allele count: 3
allele frequency: 2.471169686985173e-5
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.115+28T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.115+28T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.115+28T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.115+28T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.115+28T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.115+28T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.115+28T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.115+28T>C
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4942
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11230
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4540
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2750
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

19-9528479-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528479
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528478
    reference: chr 19
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.115+24delC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.115+24delC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.115+24delC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.115+24delC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.115+24delC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.115+24delC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.115+24delC
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.115+24delC
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11230
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1211
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51603
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: AG
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-9528480-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528480
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528480
    reference: chr 19
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.115+24C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.115+24C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.115+24C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.115+24C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.115+24C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.115+24C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.115+24C>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.115+24C>G
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11229
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1211
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1311
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

19-9528483-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528483
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528483
    reference: chr 19
allele count: 8
allele frequency: 6.589677270555675e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.115+21G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.115+21G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.115+21G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.115+21G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.115+21G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.115+21G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.115+21G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.115+21G>A
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11230
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51603
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

19-9528484-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528484
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528484
    reference: chr 19
allele count: 6
allele frequency: 4.942257952916756e-5
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.115+20C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.115+20C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.115+20C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.115+20C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.115+20C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.115+20C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.115+20C>T
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.115+20C>T
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11224
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1208
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51600
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

19-9528489-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528489
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528489
    reference: chr 19
allele count: 855
allele frequency: 7.042601561727785e-3
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.115+15A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.115+15A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.115+15A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.115+15A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.115+15A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.115+15A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.115+15A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.115+15A>G
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2493
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4948
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2691
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 11313
  bin: 9.75e1
  variant carriers: 732
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 5.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3320
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 7.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2765
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 35
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD

19-9528490-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528490
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528490
    reference: chr 19
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.115+14A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.115+14A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.115+14A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.115+14A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.115+14A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.115+14A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.115+14A>G
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.115+14A>G
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10821
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3958
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3149
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2830
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1224
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1326
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1187
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

19-9528495-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528495
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528495
    reference: chr 19
allele count: 529
allele frequency: 4.357352311291226e-3
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.115+9T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.115+9T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.115+9T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.115+9T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.115+9T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.115+9T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.115+9T>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.115+9T>A
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4932
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4989
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3905
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10898
  bin: 9.75e1
  variant carriers: 481
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4523
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1222
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51508
  bin: 9.75e1
  variant carriers: 519
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 10
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

19-9528498-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528498
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528498
    reference: chr 19
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.115+6T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.115+6T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.115+6T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.115+6T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.115+6T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.115+6T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.115+6T>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.115+6T>C
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10515
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4628
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1195
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
hgvs: c.115+6T>C
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-9528499-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528499
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528499
    reference: chr 19
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.115+5G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.115+5G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.115+5G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.115+5G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.115+5G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.115+5G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.115+5G>A
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.115+5G>A
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10515
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1341
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
hgvs: c.115+5G>A
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

19-9528501-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528501
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528501
    reference: chr 19
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.115+3G>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.115+3G>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.115+3G>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.115+3G>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.115+3G>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.115+3G>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.115+3G>C
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.115+3G>C
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10513
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2858
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1194
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 8.25e1
  variant carriers: 0
hgvs: c.115+3G>C
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-9528515-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528515
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528515
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.104G>T
  hgvsp: ENSP00000467923.1:p.Gly35Val
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.104G>T
  hgvsp: ENSP00000467315.1:p.Gly35Val
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.104G>T
  hgvsp: ENSP00000354680.2:p.Gly35Val
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.104G>T
  hgvsp: ENSP00000466714.1:p.Gly35Val
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.104G>T
  hgvsp: ENSP00000467403.1:p.Gly35Val
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.104G>T
  hgvsp: ENSP00000467151.1:p.Gly35Val
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.104G>T
  hgvsp: ENSP00000355047.1:p.Gly35Val
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.104G>T
  hgvsp: ENSP00000468491.1:p.Gly35Val
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10512
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly35Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

19-9528516-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528516
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528516
    reference: chr 19
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.103G>A
  hgvsp: ENSP00000466714.1:p.Gly35Ser
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.103G>A
  hgvsp: ENSP00000467315.1:p.Gly35Ser
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.103G>A
  hgvsp: ENSP00000467923.1:p.Gly35Ser
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.103G>A
  hgvsp: ENSP00000354680.2:p.Gly35Ser
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.103G>A
  hgvsp: ENSP00000467151.1:p.Gly35Ser
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.103G>A
  hgvsp: ENSP00000355047.1:p.Gly35Ser
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.103G>A
  hgvsp: ENSP00000468491.1:p.Gly35Ser
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.103G>A
  hgvsp: ENSP00000467403.1:p.Gly35Ser
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
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genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10512
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
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genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 9.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 51431
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly35Ser
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

19-43910616-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43910616
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 43910616
    reference: chr 19
allele count: 4
allele frequency: 3.929350281930882e-5
allele num: 101798
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131126
  ensembl protein: ENSP00000472308
  ensembl transcript: ENST00000602198
  gene symbol: TEX101
  hgvsc: ENST00000602198.1:c.-41G>C
  variant of: http://identifiers.org/hgnc/30722
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 3
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 307
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genotype depth: GenotypeDepth
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  bin: 7.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 2.5e0
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9590
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8562
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 13568
  num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

19-43910617-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43910617
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 43910617
    reference: chr 19
allele count: 1
allele frequency: 9.815276496338901e-6
allele num: 101882
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131126
  ensembl protein: ENSP00000472308
  ensembl transcript: ENST00000602198
  gene symbol: TEX101
  hgvsc: ENST00000602198.1:c.-40G>C
  variant of: http://identifiers.org/hgnc/30722
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14135
  bin: 1.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 1
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7690
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 57602
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8560
  num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/19-43910620-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43910620
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 43910620
    reference: chr 19
allele count: 4
allele frequency: 3.925108921772579e-5
allele num: 101908
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131126
  ensembl protein: ENSP00000472308
  ensembl transcript: ENST00000602198
  gene symbol: TEX101
  hgvsc: ENST00000602198.1:c.-37A>C
  variant of: http://identifiers.org/hgnc/30722
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 57612
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 13516
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 698
  num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD

19-43910622-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43910622
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 43910622
    reference: chr 19
allele count: 1
allele frequency: 9.845232938211319e-6
allele num: 101572
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131126
  ensembl protein: ENSP00000472308
  ensembl transcript: ENST00000602198
  gene symbol: TEX101
  hgvsc: ENST00000602198.1:c.-35C>T
  variant of: http://identifiers.org/hgnc/30722
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9582
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population: European (Finnish)
  type: Population
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  allele frequency: 0.0e0
  allele num: 4176
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population: East Asian
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  allele frequency: 0.0e0
  allele num: 7690
  num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
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19-43910623-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43910623
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 43910623
    reference: chr 19
allele count: 1
allele frequency: 9.825306058283716e-6
allele num: 101778
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131126
  ensembl protein: ENSP00000472308
  ensembl transcript: ENST00000602198
  gene symbol: TEX101
  hgvsc: ENST00000602198.1:c.-34G>C
  variant of: http://identifiers.org/hgnc/30722
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
  type: Population
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  allele num: 7696
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population: African
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  allele num: 8572
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population: European (Finnish)
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  allele frequency: 0.0e0
  allele num: 4174
  num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

19-43910640-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43910640
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 43910640
    reference: chr 19
allele count: 1
allele frequency: 9.767914354926936e-6
allele num: 102376
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131126
  ensembl protein: ENSP00000472308
  ensembl transcript: ENST00000602198
  gene symbol: TEX101
  hgvsc: ENST00000602198.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/30722
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 3.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: Other
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  allele num: 694
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population: European (Non-Finnish)
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  allele num: 58124
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population: Latino
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  num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
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19-43910641-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43910641
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 43910641
    reference: chr 19
allele count: 1
allele frequency: 9.764290038471303e-6
allele num: 102414
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131126
  ensembl protein: ENSP00000472308
  ensembl transcript: ENST00000602198
  gene symbol: TEX101
  hgvsc: ENST00000602198.1:c.-16C>T
  variant of: http://identifiers.org/hgnc/30722
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
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  allele num: 9820
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population: European (Finnish)
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population: South Asian
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  allele num: 12986
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
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site quality: QD
site quality: ReadPosRankSum

19-9528518-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528518
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528518
    reference: chr 19
allele count: 28
allele frequency: 2.30623507124619e-4
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.101G>C
  hgvsp: ENSP00000467403.1:p.Arg34Thr
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.101G>C
  hgvsp: ENSP00000467923.1:p.Arg34Thr
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.101G>C
  hgvsp: ENSP00000354680.2:p.Arg34Thr
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.101G>C
  hgvsp: ENSP00000467315.1:p.Arg34Thr
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.101G>C
  hgvsp: ENSP00000467151.1:p.Arg34Thr
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.101G>C
  hgvsp: ENSP00000355047.1:p.Arg34Thr
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.101G>C
  hgvsp: ENSP00000466714.1:p.Arg34Thr
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.101G>C
  hgvsp: ENSP00000468491.1:p.Arg34Thr
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4626
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10514
  bin: 9.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2860
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg34Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD

19-9528524-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528524
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528524
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.95T>C
  hgvsp: ENSP00000466714.1:p.Val32Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.95T>C
  hgvsp: ENSP00000468491.1:p.Val32Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.95T>C
  hgvsp: ENSP00000467923.1:p.Val32Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.95T>C
  hgvsp: ENSP00000355047.1:p.Val32Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.95T>C
  hgvsp: ENSP00000354680.2:p.Val32Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.95T>C
  hgvsp: ENSP00000467403.1:p.Val32Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.95T>C
  hgvsp: ENSP00000467151.1:p.Val32Ala
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.95T>C
  hgvsp: ENSP00000467315.1:p.Val32Ala
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5023
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4971
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10488
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3168
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1345
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val32Ala
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

19-9528530-C-CTAGA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 9528530
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 9528534
    reference: chr 19
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: CTAGA
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000466714
  ensembl transcript: ENST00000592904
  gene symbol: ZNF266
  hgvsc: ENST00000592904.1:c.85_88dupTCTA
  hgvsp: ENSP00000466714.1:p.Arg30IlefsTer2
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467315
  ensembl transcript: ENST00000590306
  gene symbol: ZNF266
  hgvsc: ENST00000590306.1:c.85_88dupTCTA
  hgvsp: ENSP00000467315.1:p.Arg30IlefsTer2
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467923
  ensembl transcript: ENST00000591213
  gene symbol: ZNF266
  hgvsc: ENST00000591213.1:c.85_88dupTCTA
  hgvsp: ENSP00000467923.1:p.Arg30IlefsTer2
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000468491
  ensembl transcript: ENST00000588221
  gene symbol: ZNF266
  hgvsc: ENST00000588221.1:c.85_88dupTCTA
  hgvsp: ENSP00000468491.1:p.Arg30IlefsTer2
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467151
  ensembl transcript: ENST00000588933
  gene symbol: ZNF266
  hgvsc: ENST00000588933.1:c.85_88dupTCTA
  hgvsp: ENSP00000467151.1:p.Arg30IlefsTer2
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000354680
  ensembl transcript: ENST00000361451
  gene symbol: ZNF266
  hgvsc: ENST00000361451.2:c.85_88dupTCTA
  hgvsp: ENSP00000354680.2:p.Arg30IlefsTer2
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000467403
  ensembl transcript: ENST00000592292
  gene symbol: ZNF266
  hgvsc: ENST00000592292.1:c.85_88dupTCTA
  hgvsp: ENSP00000467403.1:p.Arg30IlefsTer2
  variant of: http://identifiers.org/hgnc/13059
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000174652
  ensembl protein: ENSP00000355047
  ensembl transcript: ENST00000361151
  gene symbol: ZNF266
  hgvsc: ENST00000361151.1:c.85_88dupTCTA
  hgvsp: ENSP00000355047.1:p.Arg30IlefsTer2
  variant of: http://identifiers.org/hgnc/13059
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4971
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10487
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5023
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1229
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg30IlefsTer2
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum

19-43910642-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43910642
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 43910642
    reference: chr 19
allele count: 1
allele frequency: 9.754004018649656e-6
allele num: 102522
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000131126
  ensembl protein: ENSP00000472308
  ensembl transcript: ENST00000602198
  gene symbol: TEX101
  hgvsc: ENST00000602198.1:c.-15A>G
  variant of: http://identifiers.org/hgnc/30722
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 4714
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20192
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2825
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4364
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3522
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5665
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3874
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.55574224462491e-5
allele num: 64278
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11046
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.483e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.778e0

DP
type: SiteQuality
SIO_000300: 2.269901e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.05e-1

MQ
type: SiteQuality
SIO_000300: 5.863e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.536e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.97e-1

GenotypeQuality
all individuals: 9420
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2825
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3027
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20190
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1857
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5655
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4363
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3489
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10178
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64062
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.356e0

DP
type: SiteQuality
SIO_000300: 2.263524e6

FS
type: SiteQuality
SIO_000300: 2.428e0

VQSLOD
type: SiteQuality
SIO_000300: -1.243e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.586e0

MQRankSum
type: SiteQuality
SIO_000300: -1.889e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

QD
type: SiteQuality
SIO_000300: 1.179e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3489
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2981
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2824
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20194
bin: 9.75e1
variant carriers: 7

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5594
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4361
bin: 8.25e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63716
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

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

South Asian
type: Population
allele count: 7
allele frequency: 7.342143906020558e-4
allele num: 9534
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.304e1

MQ
type: SiteQuality
SIO_000300: 5.975e1

DP
type: SiteQuality
SIO_000300: 2.248305e6

VQSLOD
type: SiteQuality
SIO_000300: 8.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.179e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

GenotypeQuality
all individuals: 8867
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.75e1
variant carriers: 7

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5578
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2822
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9348
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.099868015838099e-4
allele num: 63644
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: 790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

DP
type: SiteQuality
SIO_000300: 2.243162e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.23e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

QD
type: SiteQuality
SIO_000300: 1.396e1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 271
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10110
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.719355650641833e-5
allele num: 63568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9234
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.984e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.217e1

DP
type: SiteQuality
SIO_000300: 2.239786e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.19e0

MQRankSum
type: SiteQuality
SIO_000300: -1.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.51e0

GenotypeQuality
all individuals: 154
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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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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
all individuals: 20193
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variant carriers: 4

GenotypeQuality
all individuals: 3838
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9196
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.979022362952701e-4
allele num: 10106
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.148515474953559e-5
allele num: 63522
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.157e1

MQ
type: SiteQuality
SIO_000300: 5.948e1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

DP
type: SiteQuality
SIO_000300: 2.23808e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

FS
type: SiteQuality
SIO_000300: 3.387e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

GenotypeQuality
all individuals: 662
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8369
bin: 6.25e1
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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variant carriers: 0

GenotypeQuality
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variant carriers: 8

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 205
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GenotypeQuality
all individuals: 3834
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variant carriers: 0

GenotypeQuality
all individuals: 99
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variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.102744257853114e-4
allele num: 63478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.093613298337708e-4
allele num: 9144
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10094
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.49e-1

FS
type: SiteQuality
SIO_000300: 2.661e0

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

DP
type: SiteQuality
SIO_000300: 2.236096e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.32e-1

QD
type: SiteQuality
SIO_000300: 1.375e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.96e-1

GenotypeQuality
all individuals: 886
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20195
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 314
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variant carriers: 0

GenotypeQuality
all individuals: 5457
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3484
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variant carriers: 0

GenotypeQuality
all individuals: 4358
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.908838684106223e-5
allele num: 10092
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63454
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9106
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.475e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e-1

QD
type: SiteQuality
SIO_000300: 1.345e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.76e-1

DP
type: SiteQuality
SIO_000300: 2.23238e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQ
type: SiteQuality
SIO_000300: 5.504e1

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

GenotypeQuality
all individuals: 340
bin: 3.25e1
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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variant carriers: 8

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
all individuals: 817
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63436
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10088
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.396288466055908e-4
allele num: 8514
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

FS
type: SiteQuality
SIO_000300: 8.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.28e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e0

QD
type: SiteQuality
SIO_000300: 1.553e1

DP
type: SiteQuality
SIO_000300: 2.23124e6

GenotypeQuality
all individuals: 5437
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 212
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8136
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.576441655894315e-5
allele num: 63434
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9086
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10088
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

QD
type: SiteQuality
SIO_000300: 1.575e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

FS
type: SiteQuality
SIO_000300: 4.058e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.231386e6

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: 5.25e1
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GenotypeQuality
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bin: 6.75e1
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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bin: 8.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 11

GenotypeQuality
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GenotypeQuality
all individuals: 835
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9086
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.15288331178863e-5
allele num: 63434
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.843820812271222e-4
allele num: 11474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10088
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.575e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.231386e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

FS
type: SiteQuality
SIO_000300: 4.058e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-1

GenotypeQuality
all individuals: 1952
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 7310
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GenotypeQuality
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GenotypeQuality
all individuals: 892
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GenotypeQuality
all individuals: 1351
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GenotypeQuality
all individuals: 3506
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GenotypeQuality
all individuals: 80
bin: 1.75e1
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GenotypeQuality
all individuals: 12078
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GenotypeQuality
all individuals: 5017
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15582
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66202
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.688044952528579e-5
allele num: 10322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.012213e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.653e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.162e0

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.988e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.8e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

QD
type: SiteQuality
SIO_000300: 1.636e1

GenotypeQuality
all individuals: 486
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15835
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12085
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7414
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.163061177017911e-4
allele num: 8598
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66312
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.08e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.61e-1

QD
type: SiteQuality
SIO_000300: 9.859999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.77e0

DP
type: SiteQuality
SIO_000300: 2.014262e6

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

GenotypeQuality
all individuals: 1809
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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: 28
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 6

GenotypeQuality
all individuals: 4002
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variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

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

Latino
type: Population
allele count: 6
allele frequency: 5.206525511975009e-4
allele num: 11524
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.606e0

VQSLOD
type: SiteQuality
SIO_000300: 4.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.41e-1

DP
type: SiteQuality
SIO_000300: 2.01673e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.78e-1

QD
type: SiteQuality
SIO_000300: 1.475e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e0

GenotypeQuality
all individuals: 5070
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18766
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3588
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1974
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1030
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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: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4000
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

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

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507477086348288e-5
allele num: 66336
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.028443e6

QD
type: SiteQuality
SIO_000300: 1.42e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.244e0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.31e0

MQ
type: SiteQuality
SIO_000300: 5.868e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: 1.31e-1

GenotypeQuality
all individuals: 393
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 350
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2651
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 561
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 303
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variant carriers: 0

GenotypeQuality
all individuals: 3611
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1983
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variant carriers: 0

GenotypeQuality
all individuals: 12095
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7618
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50665943470138e-5
allele num: 66372
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 3.812e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.94e-1

DP
type: SiteQuality
SIO_000300: 2.043452e6

QD
type: SiteQuality
SIO_000300: 1.461e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.38e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e-1

GenotypeQuality
all individuals: 249
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1982
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 2651
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 517
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variant carriers: 0

GenotypeQuality
all individuals: 102
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4030
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 2.711333373501235e-4
allele num: 66388
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.24e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

MQ
type: SiteQuality
SIO_000300: 5.99e1

QD
type: SiteQuality
SIO_000300: 1.603e1

DP
type: SiteQuality
SIO_000300: 2.046038e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7702
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
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: 10358
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504845602841149e-5
allele num: 66452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 8.015000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 7.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e0

VQSLOD
type: SiteQuality
SIO_000300: 7.47e-1

MQ
type: SiteQuality
SIO_000300: 6.07e1

DP
type: SiteQuality
SIO_000300: 2.056371e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.257e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

GenotypeQuality
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bin: 9.75e1
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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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3680
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.070908207867897e-5
allele num: 16472
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
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: 66528
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.372e1

DP
type: SiteQuality
SIO_000300: 2.060406e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.81e-1

MQ
type: SiteQuality
SIO_000300: 5.995e1

FS
type: SiteQuality
SIO_000300: 3.109e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 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: 6608
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21256214380987e-4
allele num: 16494
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

QD
type: SiteQuality
SIO_000300: 1.335e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.4e-2

FS
type: SiteQuality
SIO_000300: 4.384e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.95e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.064442e6

GenotypeQuality
all individuals: 12098
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 135
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3678
bin: 7.25e1
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GenotypeQuality
all individuals: 1
bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
all individuals: 22811
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1988
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4053
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501321162623108e-5
allele num: 66608
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.283e0

MQRankSum
type: SiteQuality
SIO_000300: -1.445e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.48e-1

FS
type: SiteQuality
SIO_000300: 4.079e0

DP
type: SiteQuality
SIO_000300: 2.065209e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 7.34e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.139999999999999e-1

GenotypeQuality
all individuals: 4050
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7815
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variant carriers: 0

GenotypeQuality
all individuals: 2663
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22935
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12101
bin: 9.75e1
variant carriers: 4

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.002400960384154e-5
allele num: 66640
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.064e0

MQRankSum
type: SiteQuality
SIO_000300: 7.25e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.99e0

QD
type: SiteQuality
SIO_000300: 1.239e1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

DP
type: SiteQuality
SIO_000300: 2.067252e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.94e-1

GenotypeQuality
all individuals: 1986
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
all individuals: 4054
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 64

GenotypeQuality
all individuals: 2660
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5139
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.730103806228374e-4
allele num: 11560
num of homozygotes: 0

African
type: Population
allele count: 58
allele frequency: 5.581216320246343e-3
allele num: 10392
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: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.00096015362458e-5
allele num: 66656
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: 16506
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

DP
type: SiteQuality
SIO_000300: 2.070231e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.54e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.17e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.86e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

QD
type: SiteQuality
SIO_000300: 1.436e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeQuality
all individuals: 1991
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 62
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4059
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2663
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5148
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 12089
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.319e0

QD
type: SiteQuality
SIO_000300: 1.551e1

DP
type: SiteQuality
SIO_000300: 2.068383e6

VQSLOD
type: SiteQuality
SIO_000300: -2.343e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

FS
type: SiteQuality
SIO_000300: 1.722e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5144
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 2664
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 12090
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7844
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1992
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4057
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3684
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.884615384615385e-4
allele num: 10400
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.12e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

FS
type: SiteQuality
SIO_000300: 4.46e-1

QD
type: SiteQuality
SIO_000300: 1.47e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.45e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-2

DP
type: SiteQuality
SIO_000300: 2.069662e6

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4059
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7850
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1991
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 23188
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5146
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 3.88e-1

QD
type: SiteQuality
SIO_000300: 1.222e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.91e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQ
type: SiteQuality
SIO_000300: 5.929e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 2.070066e6

FS
type: SiteQuality
SIO_000300: 5.327e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12093
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variant carriers: 4

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
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 5145
bin: 7.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1989
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.09e-1

QD
type: SiteQuality
SIO_000300: 1.242e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 3.535e0

DP
type: SiteQuality
SIO_000300: 2.070334e6

VQSLOD
type: SiteQuality
SIO_000300: 9.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

GenotypeQuality
all individuals: 23198
bin: 6.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4057
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1990
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12091
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2667
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5144
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3688
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.070189e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.75e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.759e-1

MQ
type: SiteQuality
SIO_000300: 5.891e1

FS
type: SiteQuality
SIO_000300: 3.274e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.05e0

MQRankSum
type: SiteQuality
SIO_000300: 1.62e0

QD
type: SiteQuality
SIO_000300: 1.024e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

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

GenotypeQuality
all individuals: 2667
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 0
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
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GenotypeQuality
all individuals: 0
bin: 2.5e0
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GenotypeQuality
all individuals: 5144
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1990
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.19e-1

MQ
type: SiteQuality
SIO_000300: 5.67e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.88e-1

QD
type: SiteQuality
SIO_000300: 5.29e0

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 2.070331e6

FS
type: SiteQuality
SIO_000300: 7.856e0

VQSLOD
type: SiteQuality
SIO_000300: 8.179999999999999e-1

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

GenotypeQuality
all individuals: 4
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variant carriers: 0

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

GenotypeQuality
all individuals: 12091
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variant carriers: 1

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 5144
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2667
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3688
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1990
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.070315e6

FS
type: SiteQuality
SIO_000300: 1.0772e1

MQRankSum
type: SiteQuality
SIO_000300: 8.34e-1

BaseQRankSum
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SIO_000300: -1.471e0

MQ
type: SiteQuality
SIO_000300: 5.641e1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -9.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.869e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

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

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

Latino
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allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.319e1

InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.977e1

DP
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SIO_000300: 2.07043e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

MQRankSum
type: SiteQuality
SIO_000300: 4.55e-1

FS
type: SiteQuality
SIO_000300: 2.206e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

GenotypeQuality
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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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variant carriers: 0

South Asian
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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: 908
num of homozygotes: 0

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

Latino
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allele count: 3
allele frequency: 2.591121091725686e-4
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e-1

FS
type: SiteQuality
SIO_000300: 9.26e-1

DP
type: SiteQuality
SIO_000300: 2.07048e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.81e-1

MQ
type: SiteQuality
SIO_000300: 5.915e1

QD
type: SiteQuality
SIO_000300: 1.038e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 45

GenotypeQuality
all individuals: 3
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 44
allele frequency: 6.593538332434214e-4
allele num: 66732
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.18e1

VQSLOD
type: SiteQuality
SIO_000300: 2.49e0

FS
type: SiteQuality
SIO_000300: 5.2e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.073756e6

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
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: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.626e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.0e-1

QD
type: SiteQuality
SIO_000300: 1.115e1

DP
type: SiteQuality
SIO_000300: 2.070018e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.21e-1

FS
type: SiteQuality
SIO_000300: 4.399e0

MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

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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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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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
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MQRankSum
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ClippingRankSum
type: SiteQuality
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VQSLOD
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QD
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MQ
type: SiteQuality
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BaseQRankSum
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DP
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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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
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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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
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

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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allele num: 16512
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.65e-1

FS
type: SiteQuality
SIO_000300: 1.024e0

DP
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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QD
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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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
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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 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

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

African
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allele frequency: 0.0e0
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East Asian
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Finnish)
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allele count: 0
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num of homozygotes: 0

VQSLOD
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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QD
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ReadPosRankSum
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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East Asian
type: Population
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allele frequency: 0.0e0
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South Asian
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allele frequency: 1.211240310077519e-4
allele num: 16512
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MQRankSum
type: SiteQuality
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MQ
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QD
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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FS
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: -3.794e0

DP
type: SiteQuality
SIO_000300: 2.06962e6

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

African
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allele count: 2
allele frequency: 1.923076923076923e-4
allele num: 10400
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.199e1

FS
type: SiteQuality
SIO_000300: 5.783e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e0

DP
type: SiteQuality
SIO_000300: 2.069511e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

MQRankSum
type: SiteQuality
SIO_000300: 6.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.175e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6612
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
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allele frequency: 6.05913717886573e-5
allele num: 16504
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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VQSLOD
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SIO_000300: -1.387e0

BaseQRankSum
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QD
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MQRankSum
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FS
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MQ
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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SIO_000300: -5.43e-1

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.067475e6

GenotypeQuality
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variant carriers: 23

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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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: 10386
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

East Asian
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allele count: 24
allele frequency: 2.776492364645997e-3
allele num: 8644
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e-1

FS
type: SiteQuality
SIO_000300: 2.923e0

DP
type: SiteQuality
SIO_000300: 2.066321e6

VQSLOD
type: SiteQuality
SIO_000300: 3.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.19e-2

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.72e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.67e-1

QD
type: SiteQuality
SIO_000300: 1.518e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6612
num of homozygotes: 0

African
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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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num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503397678753984e-5
allele num: 66516
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.054374e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.48e-1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.19e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.5496768738298e-5
allele num: 66228
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.016e0

BaseQRankSum
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QD
type: SiteQuality
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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
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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: 0
allele frequency: 0.0e0
allele num: 66228
num of homozygotes: 0

Other
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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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6600
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 1.172607879924953e-4
allele num: 8528
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.002e0

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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FS
type: SiteQuality
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MQRankSum
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DP
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MQ
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 9.682416731216112e-5
allele num: 10328
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.072e1

FS
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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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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South Asian
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num of homozygotes: 0

African
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Other
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
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East Asian
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BaseQRankSum
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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FS
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MQRankSum
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QD
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ReadPosRankSum
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ClippingRankSum
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DP
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MQ
type: SiteQuality
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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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South Asian
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num of homozygotes: 0

Latino
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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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European (Non-Finnish)
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allele num: 66728
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

African
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 3.64e-1

QD
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SIO_000300: 1.302e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

Latino
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allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.89e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.519e0

DP
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VQSLOD
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MQRankSum
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SIO_000300: 2.52e-1

FS
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QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

BaseQRankSum
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SIO_000300: 3.9e0

InbreedingCoeff
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SIO_000300: -1.0e-4

FS
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SIO_000300: 0.0e0

QD
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MQRankSum
type: SiteQuality
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MQ
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SIO_000300: 5.907e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.9e-2

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.477399e6

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
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

Latino
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allele frequency: 0.0e0
allele num: 11578
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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.69e-1

MQ
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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BaseQRankSum
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SIO_000300: -8.84e-1

QD
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DP
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InbreedingCoeff
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SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.57e-1

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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Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.833e1

MQRankSum
type: SiteQuality
SIO_000300: 2.05e-1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.477514e6

ReadPosRankSum
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SIO_000300: 1.2e0

FS
type: SiteQuality
SIO_000300: 1.418e0

BaseQRankSum
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SIO_000300: -4.016e0

VQSLOD
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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
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

East Asian
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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: 7
allele frequency: 1.048972007432716e-4
allele num: 66732
num of homozygotes: 0

QD
type: SiteQuality
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FS
type: SiteQuality
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DP
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SIO_000300: 4.478193e6

ReadPosRankSum
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MQ
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
type: SiteQuality
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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
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

East Asian
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allele count: 3
allele frequency: 3.467406380027739e-4
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
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ClippingRankSum
type: SiteQuality
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MQRankSum
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DP
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FS
type: SiteQuality
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InbreedingCoeff
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MQ
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QD
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 2.202643171806168e-3
allele num: 908
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European (Non-Finnish)
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allele count: 10
allele frequency: 1.498531439189594e-4
allele num: 66732
num of homozygotes: 0

Latino
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allele frequency: 3.109345310070824e-3
allele num: 11578
num of homozygotes: 0

African
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allele frequency: 7.543724774168749e-2
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East Asian
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allele frequency: 2.31107002542177e-3
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South Asian
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allele num: 16512
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BaseQRankSum
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DP
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VQSLOD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
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InbreedingCoeff
type: SiteQuality
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QD
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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
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

Other
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East Asian
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African
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allele frequency: 9.609840476648087e-5
allele num: 10406
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

South Asian
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MQRankSum
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
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BaseQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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FS
type: SiteQuality
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 11578
num of homozygotes: 0

South Asian
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African
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allele frequency: 4.718431674034211e-2
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European (Non-Finnish)
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allele frequency: 1.648384583108554e-4
allele num: 66732
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East Asian
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European (Finnish)
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Other
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ReadPosRankSum
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MQRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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South Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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African
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InbreedingCoeff
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BaseQRankSum
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QD
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MQRankSum
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DP
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VQSLOD
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MQ
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FS
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ReadPosRankSum
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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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African
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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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Other
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European (Finnish)
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BaseQRankSum
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InbreedingCoeff
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DP
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MQRankSum
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QD
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FS
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MQ
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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Other
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Latino
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South Asian
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African
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European (Finnish)
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InbreedingCoeff
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VQSLOD
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QD
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DP
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MQRankSum
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MQ
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ReadPosRankSum
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FS
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BaseQRankSum
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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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European (Finnish)
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Latino
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South Asian
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European (Non-Finnish)
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East Asian
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Other
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African
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BaseQRankSum
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ReadPosRankSum
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MQ
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DP
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VQSLOD
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QD
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ClippingRankSum
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FS
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InbreedingCoeff
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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East Asian
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Latino
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African
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European (Non-Finnish)
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QD
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DP
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQ
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European (Non-Finnish)
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East Asian
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Other
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European (Finnish)
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MQRankSum
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ClippingRankSum
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MQ
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DP
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ReadPosRankSum
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BaseQRankSum
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QD
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VQSLOD
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FS
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InbreedingCoeff
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South Asian
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Other
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Latino
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European (Finnish)
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ReadPosRankSum
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MQ
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ClippingRankSum
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FS
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DP
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QD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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European (Finnish)
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African
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East Asian
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Latino
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VQSLOD
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MQRankSum
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BaseQRankSum
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MQ
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ReadPosRankSum
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FS
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InbreedingCoeff
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DP
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ClippingRankSum
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QD
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South Asian
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African
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Other
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QD
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ClippingRankSum
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MQ
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FS
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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DP
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South Asian
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Other
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Latino
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European (Non-Finnish)
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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DP
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African
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East Asian
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South Asian
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European (Finnish)
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DP
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QD
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ClippingRankSum
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MQ
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FS
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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European (Non-Finnish)
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East Asian
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MQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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MQ
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FS
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ClippingRankSum
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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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South Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 28
allele frequency: 2.418379685610641e-3
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.850000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 5.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 4.402797e6

MQ
type: SiteQuality
SIO_000300: 5.9e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.318e1

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2859
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1204
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 711
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1229
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51429
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 726
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1196
bin: 7.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.397057e6

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.932e1

FS
type: SiteQuality
SIO_000300: 7.377e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.05e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.92e-2

QD
type: SiteQuality
SIO_000300: 1.172e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 710
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.95e-1

MQ
type: SiteQuality
SIO_000300: 5.348e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

DP
type: SiteQuality
SIO_000300: 4.396895e6

MQRankSum
type: SiteQuality
SIO_000300: -6.860000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.7e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.281e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.53e-1