1-16270042-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270042
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270042
    reference: chr 1
allele count: 1
allele frequency: 8.36050497450046e-6
allele num: 119610
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1577-28G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.704-28G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1577-28G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1331-28G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.265-28G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.329-28G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.247-28G>A
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2733
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1176
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

1-16270043-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270043
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270043
    reference: chr 1
allele count: 1
allele frequency: 8.3558942478024e-6
allele num: 119676
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.247-29G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1577-29G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1577-29G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.704-29G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.329-29G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.265-29G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1331-29G>A
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 2742
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum

1-16270048-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270048
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270048
    reference: chr 1
allele count: 1
allele frequency: 8.342649291709075e-6
allele num: 119866
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.265-34G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1577-34G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.247-34G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.704-34G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.329-34G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1577-34G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1331-34G>C
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31243
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9872
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 918
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1020
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 41467
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD

1-16270055-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270055
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270055
    reference: chr 1
allele count: 4
allele frequency: 3.330890680167877e-5
allele num: 120088
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.328+39C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1576+39C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1576+39C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.246+39C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.264+39C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.703+39C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1330+39C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9951
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41770
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

1-16270063-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270063
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270063
    reference: chr 1
allele count: 1
allele frequency: 8.314210648840998e-6
allele num: 120276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.703+31G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.328+31G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1576+31G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1576+31G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1330+31G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.264+31G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.246+31G>A
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9550
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41931
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 960
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

1-16270064-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270064
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270064
    reference: chr 1
allele count: 1
allele frequency: 8.315040244794785e-6
allele num: 120264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.703+30G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1330+30G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1576+30G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.328+30G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.246+30G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.264+30G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1576+30G>A
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9554
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41870
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-16270068-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270068
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270068
    reference: chr 1
allele count: 1
allele frequency: 8.310755780130645e-6
allele num: 120326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.703+26G>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1330+26G>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1576+26G>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.246+26G>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1576+26G>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.264+26G>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.328+26G>T
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42014
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2840
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

1-16270075-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270075
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270075
    reference: chr 1
allele count: 1
allele frequency: 8.305785810395521e-6
allele num: 120398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.703+19T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1576+19T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.264+19T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1330+19T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1576+19T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.328+19T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.246+19T>C
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31725
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9603
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-16270081-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270081
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270081
    reference: chr 1
allele count: 2
allele frequency: 1.660660610790973e-5
allele num: 120434
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.328+13C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.246+13C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1576+13C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1576+13C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1330+13C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.264+13C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.703+13C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9649
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10066
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2601
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42133
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum

1-16270090-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270090
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270090
    reference: chr 1
allele count: 1
allele frequency: 8.301097405076952e-6
allele num: 120466
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.703+4G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.264+4G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1576+4G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1330+4G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.328+4G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.246+4G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1576+4G>C
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2872
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
hgvs: c.1576+4G>C
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

1-16270109-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270109
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270109
    reference: chr 1
allele count: 1
allele frequency: 8.305785810395521e-6
allele num: 120398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.386G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1561G>C
  hgvsp: ENSP00000364895.4:p.Val521Leu
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1315G>C
  hgvsp: ENSP00000438529.1:p.Val439Leu
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.313G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.249G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.231G>C
  hgvsp: ENSP00000408483.1:p.Val78Leu
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.688G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1561G>C
  hgvsp: ENSP00000364885.2:p.Val521Leu
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2592
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val521Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

1-16270110-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270110
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270110
    reference: chr 1
allele count: 1
allele frequency: 8.305371914554334e-6
allele num: 120404
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1560C>T
  hgvsp: ENST00000375743.4:c.1560C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.248C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1560C>T
  hgvsp: ENST00000375733.2:c.1560C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.385C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.230C>T
  hgvsp: ENST00000444358.1:c.230C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.312C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1314C>T
  hgvsp: ENST00000537142.1:c.1314C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.687C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 9.75e1
  variant carriers: 1
hgvs: p.His520His
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-16270149-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270149
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270149
    reference: chr 1
allele count: 1
allele frequency: 8.327088017320342e-6
allele num: 120090
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.273C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1521C>T
  hgvsp: ENST00000375733.2:c.1521C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1521C>T
  hgvsp: ENST00000375743.4:c.1521C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1275C>T
  hgvsp: ENST00000537142.1:c.1275C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.346C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.209C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.191C>T
  hgvsp: ENST00000444358.1:c.191C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.648C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Cys507Cys
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

1-16270176-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270176
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270176
    reference: chr 1
allele count: 1
allele frequency: 8.364980844193866e-6
allele num: 119546
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.621G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.319G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.246G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.164G>A
  hgvsp: ENST00000444358.1:c.164G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.182G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1494G>A
  hgvsp: ENST00000375743.4:c.1494G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1494G>A
  hgvsp: ENST00000375733.2:c.1494G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1248G>A
  hgvsp: ENST00000537142.1:c.1248G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly498Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum

1-16270179-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270179
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270179
    reference: chr 1
allele count: 4
allele frequency: 3.348849670138308e-5
allele num: 119444
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.243C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.179C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.161C>T
  hgvsp: ENST00000444358.1:c.161C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.618C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1245C>T
  hgvsp: ENST00000537142.1:c.1245C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1491C>T
  hgvsp: ENST00000375743.4:c.1491C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.316C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1491C>T
  hgvsp: ENST00000375733.2:c.1491C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41623
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser497Ser
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

1-16270199-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270199
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270199
    reference: chr 1
allele count: 9
allele frequency: 7.585207160435559e-5
allele num: 118652
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.223C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.141C>A
  hgvsp: ENST00000444358.1:c.141C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1471C>A
  hgvsp: ENST00000375733.2:c.1471C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.296C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1471C>A
  hgvsp: ENST00000375743.4:c.1471C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1225C>A
  hgvsp: ENST00000537142.1:c.1225C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.159C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.598C>A
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16818
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9443
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40955
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg491Arg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD

1-16270222-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270222
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270222
    reference: chr 1
allele count: 1
allele frequency: 8.559005785887911e-6
allele num: 116836
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1460-12G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.587-12G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1460-12G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.200G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.273G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.148-12G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-12G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1214-12G>C
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2324
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8522
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3365
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-16270227-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270227
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270227
    reference: chr 1
allele count: 1
allele frequency: 8.624109560687859e-6
allele num: 115954
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1214-17C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1460-17C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-17C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.195C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.268C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.148-17C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1460-17C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.587-17C>A
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4069
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1025
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2221
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1873
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

1-16270229-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270229
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270229
    reference: chr 1
allele count: 2
allele frequency: 1.726310701400038e-5
allele num: 115854
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-19G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1460-19G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1460-19G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.193G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.266G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1214-19G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.587-19G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.148-19G>A
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17420
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4116
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1032
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

1-16270230-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270230
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270230
    reference: chr 1
allele count: 2
allele frequency: 1.725953157631302e-5
allele num: 115878
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.265C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.148-20C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.192C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1460-20C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1460-20C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1214-20C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.587-20C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-20C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6747
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27216
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7883
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4179
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2166
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

1-16270238-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270238
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270238
    reference: chr 1
allele count: 3
allele frequency: 2.615108352656078e-5
allele num: 114718
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1214-28G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.257G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.587-28G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.184G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1460-28G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-28G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.148-28G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1460-28G>A
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6144
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25603
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5132
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35749
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-16270239-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270239
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270239
    reference: chr 1
allele count: 1
allele frequency: 8.714900737280603e-6
allele num: 114746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.587-29C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1460-29C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1460-29C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.183C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.148-29C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1214-29C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-29C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.256C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17952
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4093
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7560
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5212
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2027
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1621
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

1-16270242-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270242
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270242
    reference: chr 1
allele count: 4
allele frequency: 3.50914131312068e-5
allele num: 113988
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1460-32C>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1214-32C>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1460-32C>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.253C>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.148-32C>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-32C>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.587-32C>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.180C>G
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4052
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24446
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5753
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1006
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1027
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

1-16270249-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270249
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270249
    reference: chr 1
allele count: 1
allele frequency: 8.863676653075696e-6
allele num: 112820
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.587-39T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.246T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1460-39T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1214-39T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1460-39T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-39T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.173T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.148-39T>C
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3685
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1770
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6486
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1376
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1320
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

1-16270250-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270250
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270250
    reference: chr 1
allele count: 2
allele frequency: 1.773867385674247e-5
allele num: 112748
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-40G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.148-40G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1460-40G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.245G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1214-40G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1460-40G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.172G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.587-40G>C
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5376
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22669
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17871
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1765
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 929
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1661
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6943
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1358
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

1-16270251-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270251
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270251
    reference: chr 1
allele count: 1
allele frequency: 8.899489169321681e-6
allele num: 112366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-41G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.587-41G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.171G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1460-41G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1214-41G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1460-41G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.244G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.148-41G>A
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3811
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1698
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1737
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1453
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

1-16270254-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270254
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270254
    reference: chr 1
allele count: 1
allele frequency: 8.913609298677221e-6
allele num: 112188
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-44A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1460-44A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.241A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.168A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1460-44A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.148-44A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.587-44A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1214-44A>G
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4044
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5686
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21881
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1923
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1648
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2202
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

1-16270258-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270258
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270258
    reference: chr 1
allele count: 2
allele frequency: 1.793850679869408e-5
allele num: 111492
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.147+45G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.237G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1459+45G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.586+45G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-48G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.164G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1459+45G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1213+45G>A
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5944
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1901
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1496
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1565
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31762
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

1-16270259-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270259
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270259
    reference: chr 1
allele count: 4
allele frequency: 3.598222478095821e-5
allele num: 111166
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.236C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.586+44C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-49C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.147+44C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.163C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1459+44C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1459+44C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1213+44C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 18890
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5477
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6031
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2316
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1440
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 874
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2047
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

1-16270262-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270262
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270262
    reference: chr 1
allele count: 6
allele frequency: 5.40784136998648e-5
allele num: 110950
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-52C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.160C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1459+41C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1459+41C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1213+41C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.233C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.147+41C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.586+41C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4653
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6280
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8418
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2130
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1959
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1500
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5923
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-16270264-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270264
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270265
    reference: chr 1
allele count: 2
allele frequency: 1.808285564456339e-5
allele num: 110602
alternate allele: GC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1459+38dupG
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.230dupG
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1213+38dupG
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1459+38dupG
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.157dupG
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-55dupG
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.586+38dupG
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.147+38dupG
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5697
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19913
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5856
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1315
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1472
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

1-16270265-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270265
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270265
    reference: chr 1
allele count: 5
allele frequency: 4.523331343067542e-5
allele num: 110538
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.230G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1459+38G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1459+38G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.157G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1213+38G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-55G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.147+38G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.586+38G>A
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5605
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19019
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2428
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1255
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5812
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

1-16270281-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270281
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270281
    reference: chr 1
allele count: 17
allele frequency: 1.58561381909079e-4
allele num: 107214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.586+22C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.147+22C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.141C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1459+22C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.214C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1213+22C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1459+22C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-71C>A
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7501
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17050
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19386
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6542
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3904
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2402
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2122
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29902
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

1-16270285-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270285
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270285
    reference: chr 1
allele count: 1
allele frequency: 9.405391170218769e-6
allele num: 106322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1459+18C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.137C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.210C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.586+18C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-75C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.147+18C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1459+18C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1213+18C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16248
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6572
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7788
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6840
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1882
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11502
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2810
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

1-16270289-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270289
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270289
    reference: chr 1
allele count: 1
allele frequency: 9.443405669820765e-6
allele num: 105894
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-79T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.586+14T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.147+14T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.206T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1213+14T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.133T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1459+14T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1459+14T>C
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7093
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7848
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3800
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11835
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

1-16270295-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270295
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270295
    reference: chr 1
allele count: 3
allele frequency: 2.870648575201424e-5
allele num: 104506
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1459+8C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.147+8C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.586+8C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1459+8C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.127C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.200C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1213+8C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-85C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7729
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14500
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1988
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2771
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2365
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12591
  bin: 2.25e1
  variant carriers: 0
hgvs: c.1459+8C>T
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-16270295-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270295
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270295
    reference: chr 1
allele count: 1
allele frequency: 9.568828584004747e-6
allele num: 104506
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1213+8C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.127C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.200C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1459+8C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.147+8C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1459+8C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.586+8C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-85C>A
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7729
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8131
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 903
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1980
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1988
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12591
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
hgvs: c.1459+8C>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

1-16270306-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270306
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270306
    reference: chr 1
allele count: 3
allele frequency: 2.925744602001209e-5
allele num: 102538
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-96T>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1210T>A
  hgvsp: ENSP00000438529.1:p.Ser404Thr
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.116T>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1456T>A
  hgvsp: ENSP00000364885.2:p.Ser486Thr
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.583T>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.189T>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1456T>A
  hgvsp: ENSP00000364895.4:p.Ser486Thr
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.144T>A
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22407
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8693
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4896
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3328
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13788
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser486Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

1-16270343-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270343
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270343
    reference: chr 1
allele count: 1
allele frequency: 1.126557465696325e-5
allele num: 88766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1419C>T
  hgvsp: ENST00000375733.2:c.1419C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1173C>T
  hgvsp: ENST00000537142.1:c.1173C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.107C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.79C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-133C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.152C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.*104C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.546C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1419C>T
  hgvsp: ENST00000375743.4:c.1419C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11962
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14993
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10289
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2094
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro473Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

1-16270349-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270349
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270349
    reference: chr 1
allele count: 4
allele frequency: 4.73260766682442e-5
allele num: 84520
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1413C>T
  hgvsp: ENST00000375743.4:c.1413C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.540C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.*98C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.73C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1413C>T
  hgvsp: ENST00000375733.2:c.1413C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-139C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.101C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1167C>T
  hgvsp: ENST00000537142.1:c.1167C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.146C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3335
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15172
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16663
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2321
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19924
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp471Asp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

1-16270351-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270351
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270351
    reference: chr 1
allele count: 1
allele frequency: 1.18838237391263e-5
allele num: 84148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.71G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.538G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.*96G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1165G>A
  hgvsp: ENSP00000438529.1:p.Asp389Asn
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.144G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.99G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1411G>A
  hgvsp: ENSP00000364885.2:p.Asp471Asn
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1411G>A
  hgvsp: ENSP00000364895.4:p.Asp471Asn
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-141G>A
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16965
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3179
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2089
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp471Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-16270354-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270354
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270354
    reference: chr 1
allele count: 1
allele frequency: 1.21279743857181e-5
allele num: 82454
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1408G>A
  hgvsp: ENSP00000364895.4:p.Ala470Thr
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.141G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1162G>A
  hgvsp: ENSP00000438529.1:p.Ala388Thr
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.*93G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-144G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.535G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1408G>A
  hgvsp: ENSP00000364885.2:p.Ala470Thr
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.68G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.96G>A
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13504
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2078
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26522
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1234
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala470Thr
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

1-16270355-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270355
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270355
    reference: chr 1
allele count: 1
allele frequency: 1.215539456410755e-5
allele num: 82268
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.534C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.67C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.*92C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.95C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1161C>T
  hgvsp: ENST00000537142.1:c.1161C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1407C>T
  hgvsp: ENST00000375743.4:c.1407C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1407C>T
  hgvsp: ENST00000375733.2:c.1407C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.140C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-145C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8656
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17686
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 715
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19698
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26773
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile469Ile
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

1-16270359-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270359
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270359
    reference: chr 1
allele count: 2
allele frequency: 2.492273950752667e-5
allele num: 80248
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1403A>G
  hgvsp: ENSP00000364885.2:p.His468Arg
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-149A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.91A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.*88A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1157A>G
  hgvsp: ENSP00000438529.1:p.His386Arg
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.63A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1403A>G
  hgvsp: ENSP00000364895.4:p.His468Arg
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.530A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.136A>G
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8199
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18586
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14136
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2647
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1141
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His468Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

1-16270381-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270381
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270381
    reference: chr 1
allele count: 1
allele frequency: 1.597597213790459e-5
allele num: 62594
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.*66C>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.41C>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1135C>G
  hgvsp: ENSP00000438529.1:p.Leu379Val
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-171C>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.114C>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1381C>G
  hgvsp: ENSP00000364885.2:p.Leu461Val
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.508C>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1381C>G
  hgvsp: ENSP00000364895.4:p.Leu461Val
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.69C>G
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23640
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17259
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5244
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5522
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 712
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu461Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

1-16270394-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270394
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270394
    reference: chr 1
allele count: 103
allele frequency: 1.99558259386988e-3
allele num: 51614
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-4A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-184A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.*53A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-4A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-4A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.495A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.28A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-4A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-4A>G
  variant of: http://identifiers.org/hgnc/12936
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 1.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 23743
  bin: 7.5e0
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 10236
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4743
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 15484
  bin: 1.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 32955
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1221
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 9.75e1
  variant carriers: 98
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 4
hgvs: c.1372-4A>G
num of homozygotes: 2
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

1-16270400-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270400
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270400
    reference: chr 1
allele count: 1
allele frequency: 2.140685875754592e-5
allele num: 46714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-10C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.*47C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-10C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.489C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-10C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.22C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-10C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-190C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-10C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22835
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13458
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13982
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30614
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-16270403-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270403
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270403
    reference: chr 1
allele count: 1
allele frequency: 2.405349497281955e-5
allele num: 41574
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-13T>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-13T>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-13T>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-13T>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.486T>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.19T>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.*44T>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-13T>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-193T>A
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21864
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16489
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 843
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1331
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS

1-16270405-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270405
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270405
    reference: chr 1
allele count: 1
allele frequency: 2.547511081673205e-5
allele num: 39254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-15C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.17C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-195C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-15C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-15C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-15C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.*42C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.484C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-15C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11139
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17604
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21753
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18973
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

1-16270410-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270410
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270409
    reference: chr 1
allele count: 1
allele frequency: 2.76380520700901e-5
allele num: 36182
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-21delC
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-21delC
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-21delC
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000472658
  gene symbol: ZBTB17
  hgvsc: ENST00000472658.1:n.11delC
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-21delC
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-21delC
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.*36delC
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.478delC
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-201delC
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: 3' UTR
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9921
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2996
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2263
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1418
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: AG
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

1-16270423-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270423
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270423
    reference: chr 1
allele count: 43
allele frequency: 1.623254058135145e-3
allele num: 26490
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-33G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-33G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-213G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-33G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-33G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.*24G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.466G>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-33G>C
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14530
  bin: 7.5e0
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 1.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29042
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5063
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13190
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1581
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 7.25e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-16270425-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270425
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270424
    reference: chr 1
allele count: 1
allele frequency: 4.263301500682128e-5
allele num: 23456
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.463delT
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.*21delT
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-36delT
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-216delT
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-36delT
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-36delT
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-36delT
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-36delT
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30901
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2098
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1743
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: CA
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

1-16270439-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270439
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270439
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 16528
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-49C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.*8C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-49C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.450C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-49C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-49C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-229C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-49C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 35721
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9105
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34653
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2353
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ

1-16270466-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270466
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270465
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 14450
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.422delC
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-77delC
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.1510delC
  hgvsp: ENSP00000391002.2:p.Leu504PhefsTer39
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-77delC
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-77delC
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-77delC
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-257delC
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-77delC
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: frameshift
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34477
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4428
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3605
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4114
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu504PhefsTer39
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: AG
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum

1-16270467-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270467
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270467
    reference: chr 1
allele count: 1
allele frequency: 6.948304613674263e-5
allele num: 14392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.1510C>T
  hgvsp: ENSP00000391002.2:p.Leu504Phe
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-77C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-257C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.422C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-77C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-77C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-77C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-77C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3480
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu504Phe
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

1-16270475-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270475
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270475
    reference: chr 1
allele count: 1
allele frequency: 7.111363959607453e-5
allele num: 14062
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.1502A>G
  hgvsp: ENSP00000391002.2:p.Gln501Arg
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-85A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-85A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-85A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.130-265A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.414A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-85A>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-85A>G
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31801
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2205
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3973
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2808
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln501Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: T
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ

1-16270509-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270509
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270509
    reference: chr 1
allele count: 23
allele frequency: 1.832085391110403e-3
allele num: 12554
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.1468G>A
  hgvsp: ENSP00000391002.2:p.Glu490Lys
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-119G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-119G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.380G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-119G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-119G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-119G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.129+286G>A
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 7.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18135
  bin: 2.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 9.75e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu490Lys
num of homozygotes: 1
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/1-16270511-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270511
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270511
    reference: chr 1
allele count: 21
allele frequency: 1.674641148325359e-3
allele num: 12540
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.1466T>G
  hgvsp: ENSP00000391002.2:p.Ile489Arg
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-121T>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-121T>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.129+284T>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-121T>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.378T>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-121T>G
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-121T>G
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17864
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 7.5e0
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1396
  bin: 2.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3689
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.75e1
  variant carriers: 2
hgvs: p.Ile489Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-16270516-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270516
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270516
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 12424
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-126A>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.1461A>C
  hgvsp: ENST00000448462.2:c.1461A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.129+279A>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.373A>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-126A>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-126A>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-126A>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-126A>C
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16494
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14908
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1341
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly487Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

1-16270532-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270532
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270532
    reference: chr 1
allele count: 16
allele frequency: 1.32890365448505e-3
allele num: 12040
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.129+263C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-142C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-142C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.1445C>T
  hgvsp: ENSP00000391002.2:p.Thr482Ile
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-142C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.357C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-142C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-142C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 7.5e0
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11693
  bin: 2.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3587
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1367
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr482Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum

1-16270544-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270544
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270544
    reference: chr 1
allele count: 1
allele frequency: 8.399126490844952e-5
allele num: 11906
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-154T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-154T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-154T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.129+251T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-154T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-154T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.345T>C
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.1433T>C
  hgvsp: ENSP00000391002.2:p.Leu478Pro
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9895
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 854
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu478Pro
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

1-16270546-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270546
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270546
    reference: chr 1
allele count: 1
allele frequency: 8.437394532568343e-5
allele num: 11852
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-156G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-156G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-156G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.343G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-156G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.129+249G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-156G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.1431G>A
  hgvsp: ENST00000448462.2:c.1431G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9732
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro477Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

1-16270566-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270566
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270566
    reference: chr 1
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-176G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-176G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-176G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.323G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-176G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.1411G>A
  hgvsp: ENSP00000391002.2:p.Gly471Arg
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.129+229G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-176G>A
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6871
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly471Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/1-16270583-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270583
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270582
    reference: chr 1
allele count: 1
allele frequency: 8.673026886383348e-5
allele num: 11530
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.129+211delG
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1372-194delG
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.105-194delG
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.60-194delG
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.305delG
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1126-194delG
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.1393delG
  hgvsp: ENSP00000391002.2:p.Val465SerfsTer2
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1372-194delG
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4897
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val465SerfsTer2
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
reference allele: AC
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-16270637-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270637
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270637
    reference: chr 1
allele count: 2
allele frequency: 1.696352841391009e-4
allele num: 11790
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1371+158G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.59+158G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1371+158G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.104+158G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.252G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.1340G>A
  hgvsp: ENSP00000391002.2:p.Arg447Gln
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1125+158G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.129+158G>A
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 653
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4536
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1020
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg447Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD

1-16270638-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270638
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270638
    reference: chr 1
allele count: 2
allele frequency: 1.694628029147602e-4
allele num: 11802
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.104+157C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.251C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.1339C>T
  hgvsp: ENSP00000391002.2:p.Arg447Trp
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1125+157C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1371+157C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.129+157C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1371+157C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.59+157C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1016
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4610
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg447Trp
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD

1-16270639-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270639
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270639
    reference: chr 1
allele count: 2
allele frequency: 1.687763713080169e-4
allele num: 11850
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.250G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1371+156G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1125+156G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.104+156G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.129+156G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.1338G>A
  hgvsp: ENST00000448462.2:c.1338G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1371+156G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.59+156G>A
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5379
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 633
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1041
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro446Pro
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

1-16270667-CTGGGTGAACAAGCTGA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270667
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270651
    reference: chr 1
allele count: 134
allele frequency: 1.048841577958673e-2
allele num: 12776
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsp: ENSP00000391002.2:p.Ser432GlyfsTer30
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 2.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 2.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 7.5e0
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 6817
  bin: 2.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 3.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6141
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1345
  bin: 2.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser432GlyfsTer30
num of homozygotes: 2
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: CTGGGTGAACAAGCTGA
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

1-16270687-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270687
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270687
    reference: chr 1
allele count: 4
allele frequency: 2.968239833778569e-4
allele num: 13476
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.59+108C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.104+108C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.129+108C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1371+108C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.1290C>T
  hgvsp: ENST00000448462.2:c.1290C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.202C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1125+108C>T
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1371+108C>T
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8330
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4163
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 944
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser430Ser
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

1-16270699-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270699
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270699
    reference: chr 1
allele count: 1
allele frequency: 7.187005893344832e-5
allele num: 13914
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.104+96G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1371+96G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.129+96G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1125+96G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1371+96G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.190G>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.1278G>A
  hgvsp: ENST00000448462.2:c.1278G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.59+96G>A
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9799
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro426Pro
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

1-16270703-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 16270703
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 16270703
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 14470
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000438529
  ensembl transcript: ENST00000537142
  gene symbol: ZBTB17
  hgvsc: ENST00000537142.1:c.1125+92C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000474511
  gene symbol: ZBTB17
  hgvsc: ENST00000474511.1:n.186C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000487785
  gene symbol: ZBTB17
  hgvsc: ENST00000487785.1:n.104+92C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000391002
  ensembl transcript: ENST00000448462
  gene symbol: ZBTB17
  hgvsc: ENST00000448462.2:c.1274C>A
  hgvsp: ENSP00000391002.2:p.Ala425Asp
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364885
  ensembl transcript: ENST00000375733
  gene symbol: ZBTB17
  hgvsc: ENST00000375733.2:c.1371+92C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl transcript: ENST00000471805
  gene symbol: ZBTB17
  hgvsc: ENST00000471805.1:n.59+92C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000408483
  ensembl transcript: ENST00000444358
  gene symbol: ZBTB17
  hgvsc: ENST00000444358.1:c.129+92C>A
  variant of: http://identifiers.org/hgnc/12936
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116809
  ensembl protein: ENSP00000364895
  ensembl transcript: ENST00000375743
  gene symbol: ZBTB17
  hgvsc: ENST00000375743.4:c.1371+92C>A
  variant of: http://identifiers.org/hgnc/12936
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10496
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala425Asp
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 9805
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2492
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 110
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41318
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.678668215253581e-5
allele num: 10332
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15734
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65890
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 7.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 1.342e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

DP
type: SiteQuality
SIO_000300: 1.586497e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.75e-1

QD
type: SiteQuality
SIO_000300: 1.428e1

GenotypeQuality
all individuals: 9817
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2507
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41314
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 224
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1157
bin: 2.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65910
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.659508139937652e-5
allele num: 11548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15772
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
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: 8620
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.912e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.154e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.456e1

DP
type: SiteQuality
SIO_000300: 1.586958e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.132e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.11e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 285
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15932
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
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: 1
allele frequency: 1.516346212167162e-5
allele num: 65948
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.616e0

FS
type: SiteQuality
SIO_000300: 1.5445e1

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

DP
type: SiteQuality
SIO_000300: 1.591187e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.124e0

QD
type: SiteQuality
SIO_000300: 1.353e1

GenotypeQuality
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bin: 2.25e1
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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variant carriers: 4

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
allele num: 896
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16110
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.596503375454388e-4
allele num: 11554
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515518913676043e-5
allele num: 65984
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.3e-2

MQ
type: SiteQuality
SIO_000300: 5.98e1

FS
type: SiteQuality
SIO_000300: 1.1173e1

DP
type: SiteQuality
SIO_000300: 1.596343e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.0e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.767e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.69e-1

QD
type: SiteQuality
SIO_000300: 1.083e1

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
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: 1
allele frequency: 6.152331733727083e-5
allele num: 16254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66024
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.65e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 1.427e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.15e-1

DP
type: SiteQuality
SIO_000300: 1.600248e6

QD
type: SiteQuality
SIO_000300: 1.483e1

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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bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514921981517952e-5
allele num: 66010
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
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allele count: 0
allele frequency: 0.0e0
allele num: 16260
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.666e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.61e0

QD
type: SiteQuality
SIO_000300: 1.06e1

MQRankSum
type: SiteQuality
SIO_000300: -1.522e0

DP
type: SiteQuality
SIO_000300: 1.600576e6

VQSLOD
type: SiteQuality
SIO_000300: -3.108e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.79e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.93e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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: 8616
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514784294716432e-5
allele num: 66016
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16322
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.538e0

VQSLOD
type: SiteQuality
SIO_000300: 3.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.761e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.706e0

QD
type: SiteQuality
SIO_000300: 9.67e0

DP
type: SiteQuality
SIO_000300: 1.601459e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.682416731216112e-5
allele num: 10328
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66014
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.817e0

DP
type: SiteQuality
SIO_000300: 1.602947e6

MQ
type: SiteQuality
SIO_000300: 5.855e1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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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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: 66010
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.321262766945218e-4
allele num: 8616
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.979e1

MQRankSum
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.350000000000001e-1

DP
type: SiteQuality
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QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.870000000000001e-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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variant carriers: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16486
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
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: 1
allele frequency: 1.514738404677512e-5
allele num: 66018
num of homozygotes: 0

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
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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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

African
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allele count: 0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 8.670019074041963e-5
allele num: 11534
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South Asian
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66012
num of homozygotes: 0

InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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QD
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DP
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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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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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.162250116225012e-4
allele num: 8604
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66016
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.964e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.79e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.489e0

QD
type: SiteQuality
SIO_000300: 1.315e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.8138e1

DP
type: SiteQuality
SIO_000300: 1.604617e6

MQRankSum
type: SiteQuality
SIO_000300: 8.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-1

GenotypeQuality
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bin: 3.75e1
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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bin: 5.25e1
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GenotypeQuality
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bin: 2.25e1
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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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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51828009231143e-5
allele num: 65864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.536e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.06e-1

DP
type: SiteQuality
SIO_000300: 1.597923e6

FS
type: SiteQuality
SIO_000300: 1.3803e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.903e0

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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bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10144
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6426
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16795141322121e-4
allele num: 8562
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: -5.423e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

QD
type: SiteQuality
SIO_000300: 7.26e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.1e0

DP
type: SiteQuality
SIO_000300: 1.583978e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.873617693522907e-5
allele num: 10128
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.578614816397546e-5
allele num: 65522
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.580852e6

QD
type: SiteQuality
SIO_000300: 1.144e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.44e-1

FS
type: SiteQuality
SIO_000300: 1.5666e1

MQ
type: SiteQuality
SIO_000300: 5.972e1

VQSLOD
type: SiteQuality
SIO_000300: -1.136e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e0

GenotypeQuality
all individuals: 60
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 226
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6256
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.382148780637631e-4
allele num: 65116
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10032
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-1

DP
type: SiteQuality
SIO_000300: 1.556996e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 2.668e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.04e-1

QD
type: SiteQuality
SIO_000300: 1.424e1

GenotypeQuality
all individuals: 38602
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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: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.556420233463035e-5
allele num: 64250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11272
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6004
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16230
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.263e1

FS
type: SiteQuality
SIO_000300: 1.366e0

MQRankSum
type: SiteQuality
SIO_000300: 4.67e-1

DP
type: SiteQuality
SIO_000300: 1.496991e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.827e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.11e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e0

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
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5920
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9676
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8396
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.567348985925206e-5
allele num: 63802
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.46786e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.769e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.427e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.25e-1

QD
type: SiteQuality
SIO_000300: 8.43e0

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: 1.03476821192053e-4
allele num: 9664
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5900
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11188
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.568676664365941e-5
allele num: 63748
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.889e1

FS
type: SiteQuality
SIO_000300: 1.269e0

VQSLOD
type: SiteQuality
SIO_000300: -8.971e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

DP
type: SiteQuality
SIO_000300: 1.465881e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.17e-1

QD
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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GenotypeQuality
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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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63756
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.241002730206007e-4
allele num: 16116
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Other
type: Population
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allele num: 854
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8392
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5918
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -9.314e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.595e0

FS
type: SiteQuality
SIO_000300: 9.654999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

DP
type: SiteQuality
SIO_000300: 1.464004e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.428e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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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: 3
allele frequency: 4.749089757796423e-5
allele num: 63170
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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Other
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ReadPosRankSum
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MQ
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FS
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QD
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MQRankSum
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VQSLOD
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BaseQRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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SIO_000300: 1.37e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 1.582528881152081e-5
allele num: 63190
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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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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Other
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allele frequency: 0.0e0
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South Asian
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allele frequency: 2.515090543259558e-4
allele num: 15904
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BaseQRankSum
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FS
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MQRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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MQ
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QD
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0.0e0
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Other
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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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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.607975558771507e-5
allele num: 62190
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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DP
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SIO_000300: 1.370186e6

VQSLOD
type: SiteQuality
SIO_000300: 6.43e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.97e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.81e-1

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.215744284014535e-5
allele num: 62194
num of homozygotes: 0

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

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

FS
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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MQRankSum
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SIO_000300: 1.51e-1

QD
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BaseQRankSum
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SIO_000300: 2.61e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 834
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele num: 8138
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Latino
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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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African
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South Asian
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FS
type: SiteQuality
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QD
type: SiteQuality
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DP
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BaseQRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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South Asian
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Other
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African
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Latino
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European (Non-Finnish)
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allele num: 61888
num of homozygotes: 0

MQ
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QD
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BaseQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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Other
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East Asian
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European (Non-Finnish)
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Latino
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South Asian
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BaseQRankSum
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FS
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MQRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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VQSLOD
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MQ
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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East Asian
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South Asian
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Latino
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European (Non-Finnish)
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Other
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MQRankSum
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FS
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VQSLOD
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MQ
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BaseQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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allele frequency: 3.846153846153846e-4
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European (Finnish)
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East Asian
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allele frequency: 0.0e0
allele num: 8020
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10614
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.7e-2

MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.717e0

MQRankSum
type: SiteQuality
SIO_000300: 6.39e-1

DP
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ClippingRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.098e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.57e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15564
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.635965055786408e-5
allele num: 61126
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 7986
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 10568
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.086248099065827e-4
allele num: 9206
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5346
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.514e0

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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MQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.45e-1

ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.209e1

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
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allele count: 0
allele frequency: 0.0e0
allele num: 10564
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7988
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.18491356731273e-5
allele num: 61088
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 7.74e-1

QD
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InbreedingCoeff
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SIO_000300: -1.3e-3

ClippingRankSum
type: SiteQuality
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FS
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BaseQRankSum
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SIO_000300: -2.163e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

DP
type: SiteQuality
SIO_000300: 1.310898e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59308
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele count: 16
allele frequency: 1.788908765652952e-3
allele num: 8944
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5062
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 9.84251968503937e-5
allele num: 10160
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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QD
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.247993e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.27e-1

FS
type: SiteQuality
SIO_000300: 2.459e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.398e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 1
allele frequency: 1.698600353308873e-5
allele num: 58872
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15128
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10084
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4954
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7646
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.55e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.23169e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.85e0

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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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 58654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10028
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.308557969118032e-4
allele num: 7642
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8830
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4904
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.154e0

MQRankSum
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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QD
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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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Other
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allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.015847216578627e-4
allele num: 9844
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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 frequency: 0.0e0
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African
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allele frequency: 2.295157218269452e-4
allele num: 8714
num of homozygotes: 0

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

East Asian
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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European (Finnish)
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African
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allele num: 8714
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South Asian
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Other
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InbreedingCoeff
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ReadPosRankSum
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MQ
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FS
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MQRankSum
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QD
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VQSLOD
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DP
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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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Latino
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East Asian
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele num: 56874
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African
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Other
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ClippingRankSum
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QD
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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FS
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VQSLOD
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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European (Non-Finnish)
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allele count: 1
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allele num: 48904
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African
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East Asian
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allele frequency: 0.0e0
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Other
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Latino
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allele frequency: 0.0e0
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MQ
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InbreedingCoeff
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BaseQRankSum
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FS
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ClippingRankSum
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DP
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VQSLOD
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MQRankSum
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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allele frequency: 0.0e0
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Other
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 8.590696275933165e-5
allele num: 46562
num of homozygotes: 0

South Asian
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African
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allele frequency: 0.0e0
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Latino
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MQ
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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MQRankSum
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FS
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BaseQRankSum
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QD
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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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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African
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allele frequency: 0.0e0
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East Asian
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allele num: 6018
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European (Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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DP
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FS
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QD
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MQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 9.79e-1

ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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allele num: 45354
num of homozygotes: 0

South Asian
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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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Other
type: Population
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allele frequency: 0.0e0
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QD
type: SiteQuality
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InbreedingCoeff
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MQ
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MQRankSum
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DP
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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FS
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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allele frequency: 0.0e0
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Latino
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Other
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.21004243281471e-5
allele num: 45248
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European (Finnish)
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MQRankSum
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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MQ
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FS
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ReadPosRankSum
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DP
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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num of homozygotes: 0

African
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Latino
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East Asian
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Other
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European (Finnish)
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allele num: 3138
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South Asian
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InbreedingCoeff
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QD
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DP
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FS
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VQSLOD
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ReadPosRankSum
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MQRankSum
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MQ
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

European (Finnish)
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Other
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European (Non-Finnish)
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African
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Latino
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South Asian
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InbreedingCoeff
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ReadPosRankSum
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DP
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QD
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MQ
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MQRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Latino
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European (Finnish)
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Other
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East Asian
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South Asian
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DP
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ClippingRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQ
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Other
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African
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Latino
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VQSLOD
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MQ
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FS
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BaseQRankSum
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DP
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InbreedingCoeff
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QD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

GenotypeQuality
all individuals: 17749
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 253
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1415
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2752
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6192
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26157
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.646903123345686e-4
allele num: 3778
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-1

DP
type: SiteQuality
SIO_000300: 5.7399e5

QD
type: SiteQuality
SIO_000300: 1.181e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.4e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 3074
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1489
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 151
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24653
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1104
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1287
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 298
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6071
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2238
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.791736460078169e-4
allele num: 3582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20070
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2588
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 922
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.238e-1

QD
type: SiteQuality
SIO_000300: 1.277e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.532e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

DP
type: SiteQuality
SIO_000300: 5.60405e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.82e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 23785
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1180
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 40
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5944
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20834
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18254
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1946
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.969121140142518e-4
allele num: 3368
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9334
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2230
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.668e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.29e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.40227e5

MQRankSum
type: SiteQuality
SIO_000300: 3.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.098e0

QD
type: SiteQuality
SIO_000300: 6.16e0

VQSLOD
type: SiteQuality
SIO_000300: -9.162e-1

MQ
type: SiteQuality
SIO_000300: 6.083e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

GenotypeQuality
all individuals: 290
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1512
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 31431
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1455
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 285
bin: 3.25e1
variant carriers: 6

GenotypeQuality
all individuals: 92
bin: 9.75e1
variant carriers: 61

GenotypeQuality
all individuals: 31
bin: 9.25e1
variant carriers: 5

GenotypeQuality
all individuals: 41
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 3

African
type: Population
allele count: 1
allele frequency: 4.166666666666667e-4
allele num: 2400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 36
allele frequency: 2.896684905053106e-3
allele num: 12428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1174
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 5.728689275893675e-4
allele num: 8728
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.517887563884157e-4
allele num: 1174
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 362
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

FS
type: SiteQuality
SIO_000300: 3.219e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.322e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.84e-2

DP
type: SiteQuality
SIO_000300: 4.36561e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e-1

GenotypeQuality
all individuals: 287
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 937
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32521
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10530
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4784
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 986
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10494
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.096491228070175e-3
allele num: 912
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2118
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.18e-1

QD
type: SiteQuality
SIO_000300: 1.546e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.54e0

MQ
type: SiteQuality
SIO_000300: 6.153e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.78e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

DP
type: SiteQuality
SIO_000300: 4.106e5

VQSLOD
type: SiteQuality
SIO_000300: 3.15e0

GenotypeQuality
all individuals: 288
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6746
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4456
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 125
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 143
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 398
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7974
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6100
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 164
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.09e0

DP
type: SiteQuality
SIO_000300: 3.39715e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.679999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.518e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 484
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2200
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32853
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 36
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 309
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 921
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 272
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7852
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4830
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 970
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 348
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.720000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.409999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.178e1

VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

DP
type: SiteQuality
SIO_000300: 2.82742e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

GenotypeQuality
all individuals: 32428
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2318
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4109
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 962
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.27420998980632e-4
allele num: 7848
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 150
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.80386e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.48e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.856e1

FS
type: SiteQuality
SIO_000300: 1.116e0

MQRankSum
type: SiteQuality
SIO_000300: 4.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: -1.086e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.897e0

GenotypeQuality
all individuals: 330
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 202
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30150
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.275835672365399e-4
allele num: 7838
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 256
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 332
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 914
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.426e1

FS
type: SiteQuality
SIO_000300: 3.975e0

VQSLOD
type: SiteQuality
SIO_000300: -1.476e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.550000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.94e-1

DP
type: SiteQuality
SIO_000300: 2.64707e5

MQ
type: SiteQuality
SIO_000300: 5.928e1

GenotypeQuality
all individuals: 3694
bin: 6.25e1
variant carriers: 2

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1389
bin: 2.25e1
variant carriers: 4

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

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

African
type: Population
allele count: 22
allele frequency: 3.536977491961415e-2
allele num: 622
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.774694783573807e-4
allele num: 3604
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7760
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.7e-2

DP
type: SiteQuality
SIO_000300: 2.04412e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 1.755e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.311e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 23

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 1

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

African
type: Population
allele count: 20
allele frequency: 3.257328990228013e-2
allele num: 614
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3590
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.287664177182591e-4
allele num: 7766
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-2

DP
type: SiteQuality
SIO_000300: 2.0359e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.48e1

VQSLOD
type: SiteQuality
SIO_000300: 3.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.969999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.16e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 57
bin: 9.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7760
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.387e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 1.98502e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.84e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.063e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.27e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 16

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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bin: 3.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7728
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

African
type: Population
allele count: 16
allele frequency: 3.162055335968379e-2
allele num: 506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3282
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

QD
type: SiteQuality
SIO_000300: 1.228e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-2

DP
type: SiteQuality
SIO_000300: 1.82561e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.68e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.27e0

FS
type: SiteQuality
SIO_000300: 1.127e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 75
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GenotypeQuality
all individuals: 375
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7714
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.111387678904792e-4
allele num: 3214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.607e0

VQSLOD
type: SiteQuality
SIO_000300: -4.617e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.26e0

DP
type: SiteQuality
SIO_000300: 1.76034e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.051e0

MQRankSum
type: SiteQuality
SIO_000300: 9.21e-1

QD
type: SiteQuality
SIO_000300: 8.789999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.710000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.302e0

MQ
type: SiteQuality
SIO_000300: 5.854e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 832
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.298364061282784e-4
allele num: 7702
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 156
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.928e0

MQRankSum
type: SiteQuality
SIO_000300: -1.567e0

FS
type: SiteQuality
SIO_000300: 1.036e0

DP
type: SiteQuality
SIO_000300: 1.75428e5

QD
type: SiteQuality
SIO_000300: 1.09e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.81e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.283e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.69e-2

MQ
type: SiteQuality
SIO_000300: 5.939e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.81e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 679
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3010
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.303441084462982e-4
allele num: 7672
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.92e-2

DP
type: SiteQuality
SIO_000300: 1.65919e5

FS
type: SiteQuality
SIO_000300: 2.549e0

QD
type: SiteQuality
SIO_000300: 1.306e1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQ
type: SiteQuality
SIO_000300: 5.869e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.111e0

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
all individuals: 600
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 57
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2990
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.304121022430882e-4
allele num: 7668
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.43e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.64e-1

DP
type: SiteQuality
SIO_000300: 1.62475e5

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

MQRankSum
type: SiteQuality
SIO_000300: -2.306e0

QD
type: SiteQuality
SIO_000300: 1.29e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.065e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 370
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GenotypeQuality
all individuals: 61
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3110
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.600780234070221e-4
allele num: 7690
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 512
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.9e-2

MQ
type: SiteQuality
SIO_000300: 5.943e1

VQSLOD
type: SiteQuality
SIO_000300: -1.014e0

DP
type: SiteQuality
SIO_000300: 1.67451e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.07e-2

FS
type: SiteQuality
SIO_000300: 3.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.09e0

QD
type: SiteQuality
SIO_000300: 1.398e1

GenotypeQuality
all individuals: 47
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GenotypeQuality
all individuals: 661
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GenotypeQuality
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GenotypeQuality
all individuals: 22
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 102
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GenotypeQuality
all individuals: 318
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 175
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3627
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3118
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 160
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 516
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.599428125812321e-4
allele num: 7694
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.14e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.134e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.18e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e-1

DP
type: SiteQuality
SIO_000300: 1.67979e5

FS
type: SiteQuality
SIO_000300: 2.868e0

QD
type: SiteQuality
SIO_000300: 1.373e1

GenotypeQuality
all individuals: 62
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4743
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 869
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3648
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 103
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.595380223202699e-4
allele num: 7706
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3136
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.501e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.285e0

FS
type: SiteQuality
SIO_000300: 1.281e0

QD
type: SiteQuality
SIO_000300: 1.287e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.23e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.167e0

DP
type: SiteQuality
SIO_000300: 1.68711e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeQuality
all individuals: 81
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 5

GenotypeQuality
all individuals: 229
bin: 9.75e1
variant carriers: 171

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3622
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 238
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 2.142857142857143e-2
allele num: 140
num of homozygotes: 0

African
type: Population
allele count: 128
allele frequency: 1.620253164556962e-1
allele num: 790
num of homozygotes: 2

Latino
type: Population
allele count: 2
allele frequency: 9.615384615384616e-3
allele num: 208
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.28633907898122e-4
allele num: 7774
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.12e-1

QD
type: SiteQuality
SIO_000300: 2.66e0

DP
type: SiteQuality
SIO_000300: 1.85759e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.42e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.637e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.12e-1

MQ
type: SiteQuality
SIO_000300: 5.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.671e-1

GenotypeQuality
all individuals: 1426
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 4
allele frequency: 5.119017148707448e-4
allele num: 7814
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4128
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 262
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 228
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.67e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.873e0

VQSLOD
type: SiteQuality
SIO_000300: -7.904e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.43e-1

DP
type: SiteQuality
SIO_000300: 1.96672e5

MQ
type: SiteQuality
SIO_000300: 5.936e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-1

QD
type: SiteQuality
SIO_000300: 8.869999999999999e0

GenotypeQuality
all individuals: 4341
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1171
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 93
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 358
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variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 966
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.276813074565884e-4
allele num: 7832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4438
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

VQSLOD
type: SiteQuality
SIO_000300: -2.093e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

MQRankSum
type: SiteQuality
SIO_000300: -8.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.95e-2

QD
type: SiteQuality
SIO_000300: 1.149e1

DP
type: SiteQuality
SIO_000300: 2.05076e5