16-71512092-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512092
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512092
    reference: chr 16
allele count: 64
allele frequency: 7.039000461934405e-4
allele num: 90922
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.274+39T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.274+39T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.*31T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.148+39T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.274+39T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.274+39T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*155+39T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*231+39T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.64+39T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.274+39T>C
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5011
  bin: 1.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16873
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 4057
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 13714
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15168
  bin: 2.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1856
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-71512095-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512095
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512095
    reference: chr 16
allele count: 1
allele frequency: 1.092991736982468e-5
allele num: 91492
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.*28G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.274+36G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.274+36G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.148+36G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.64+36G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*155+36G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.274+36G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*231+36G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.274+36G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.274+36G>A
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3809
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18014
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 1.75e1
  variant carriers: 0
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: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP

16-71512099-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512099
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512099
    reference: chr 16
allele count: 1
allele frequency: 1.062496015639941e-5
allele num: 94118
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.*24T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.274+32T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.274+32T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*155+32T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*231+32T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.274+32T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.274+32T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.64+32T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.148+32T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.274+32T>C
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12800
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: A
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-71512101-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512101
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512101
    reference: chr 16
allele count: 10
allele frequency: 1.04782262458611e-4
allele num: 95436
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.148+30T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.274+30T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*155+30T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.*22T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.64+30T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.274+30T>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.274+30T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.274+30T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.274+30T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*231+30T>G
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5335
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25523
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10042
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1917
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 3371
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

16-71512104-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512104
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512104
    reference: chr 16
allele count: 3
allele frequency: 3.084706027515578e-5
allele num: 97254
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.274+27A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.274+27A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.148+27A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*155+27A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.*19A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.274+27A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.64+27A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.274+27A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*231+27A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.274+27A>G
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-71512106-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512106
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512106
    reference: chr 16
allele count: 1
allele frequency: 1.015145977991635e-5
allele num: 98508
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*155+25A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.64+25A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.274+25A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.274+25A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.274+25A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.*17A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.274+25A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.148+25A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*231+25A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.274+25A>C
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10958
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7680
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5850
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2711
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS

16-71512107-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512107
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512107
    reference: chr 16
allele count: 1
allele frequency: 1.007759750075582e-5
allele num: 99230
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.274+24A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.*16A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*231+24A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*155+24A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.274+24A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.274+24A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.64+24A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.274+24A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.274+24A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.148+24A>C
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5952
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10630
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

16-71512112-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512112
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512112
    reference: chr 16
allele count: 3
allele frequency: 2.922153822177199e-5
allele num: 102664
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.274+19G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.274+19G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.274+19G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.274+19G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*155+19G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.*11G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.274+19G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.64+19G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*231+19G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.148+19G>A
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9007
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32868
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1913
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-71512127-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512127
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512127
    reference: chr 16
allele count: 1
allele frequency: 8.855199773306886e-6
allele num: 112928
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.274+4G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.274+4G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.274+4G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*231+4G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.239G>A
  hgvsp: ENSP00000462021.1:p.Arg80Lys
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.274+4G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.274+4G>A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.148+4G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*155+4G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.64+4G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.870G>A
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg80Lys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

16-71512140-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512140
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512140
    reference: chr 16
allele count: 1
allele frequency: 8.553880895762407e-6
allele num: 116906
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.265G>A
  hgvsp: ENSP00000288177.5:p.Val89Ile
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.265G>A
  hgvsp: ENSP00000462566.1:p.Val89Ile
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.857G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.139G>A
  hgvsp: ENSP00000454864.1:p.Val47Ile
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.55G>A
  hgvsp: ENSP00000462810.1:p.Val19Ile
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.265G>A
  hgvsp: ENSP00000463741.1:p.Val89Ile
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.226G>A
  hgvsp: ENSP00000462021.1:p.Val76Ile
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*222G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.265G>A
  hgvsp: ENSP00000455796.1:p.Val89Ile
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.265G>A
  hgvsp: ENSP00000458105.1:p.Val89Ile
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*146G>A
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val89Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-71512141-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512141
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512141
    reference: chr 16
allele count: 1
allele frequency: 8.53344256139812e-6
allele num: 117186
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.225C>T
  hgvsp: ENST00000561469.1:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.264C>T
  hgvsp: ENST00000567225.1:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.264C>T
  hgvsp: ENST00000568815.1:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.138C>T
  hgvsp: ENST00000565637.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.856C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.264C>T
  hgvsp: ENST00000564230.1:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*221C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.264C>T
  hgvsp: ENST00000288177.5:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.54C>T
  hgvsp: ENST00000565100.2:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.264C>T
  hgvsp: ENST00000561908.1:c.264C>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*145C>T
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn88Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

16-71512147-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512147
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512147
    reference: chr 16
allele count: 1
allele frequency: 8.464676903282601e-6
allele num: 118138
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*139C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.850C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*215C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.48C>T
  hgvsp: ENST00000565100.2:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.219C>T
  hgvsp: ENST00000561469.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.258C>T
  hgvsp: ENST00000288177.5:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.258C>T
  hgvsp: ENST00000568815.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.258C>T
  hgvsp: ENST00000567225.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.258C>T
  hgvsp: ENST00000561908.1:c.258C>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.132C>T
  hgvsp: ENST00000565637.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.258C>T
  hgvsp: ENST00000564230.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr86Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

16-71512162-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512162
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512162
    reference: chr 16
allele count: 2
allele frequency: 1.673668178546921e-5
allele num: 119498
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.204C>T
  hgvsp: ENST00000561469.1:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.835C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*200C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.243C>T
  hgvsp: ENST00000561908.1:c.243C>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.243C>T
  hgvsp: ENST00000564230.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.243C>T
  hgvsp: ENST00000568815.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.117C>T
  hgvsp: ENST00000565637.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.243C>T
  hgvsp: ENST00000288177.5:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.33C>T
  hgvsp: ENST00000565100.2:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.243C>T
  hgvsp: ENST00000567225.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*124C>T
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro81Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum

16-71512174-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512174
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512174
    reference: chr 16
allele count: 2
allele frequency: 1.669142561466175e-5
allele num: 119822
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*112A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.21A>C
  hgvsp: ENST00000565100.2:c.21A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.192A>C
  hgvsp: ENST00000561469.1:c.192A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.231A>C
  hgvsp: ENST00000564230.1:c.231A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*188A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.231A>C
  hgvsp: ENST00000288177.5:c.231A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.231A>C
  hgvsp: ENST00000568815.1:c.231A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.231A>C
  hgvsp: ENST00000567225.1:c.231A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.231A>C
  hgvsp: ENST00000561908.1:c.231A>C(p.%3D)
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.823A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.105A>C
  hgvsp: ENST00000565637.1:c.105A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala77Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

16-71512175-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512175
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512176
    reference: chr 16
allele count: 127
allele frequency: 1.059534138690516e-3
allele num: 119864
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.103dupG
  hgvsp: ENSP00000454864.1:p.Ala35GlyfsTer4
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.229dupG
  hgvsp: ENSP00000462566.1:p.Ala77GlyfsTer4
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.229dupG
  hgvsp: ENSP00000458105.1:p.Ala77GlyfsTer4
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.229dupG
  hgvsp: ENSP00000463741.1:p.Ala77GlyfsTer4
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*186dupG
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.19dupG
  hgvsp: ENSP00000462810.1:p.Ala7GlyfsTer4
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.229dupG
  hgvsp: ENSP00000288177.5:p.Ala77GlyfsTer4
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.190dupG
  hgvsp: ENSP00000462021.1:p.Ala64GlyfsTer4
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.821dupG
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.229dupG
  hgvsp: ENSP00000455796.1:p.Ala77GlyfsTer4
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*110dupG
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11187
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 42198
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2926
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Ala77GlyfsTer4
num of homozygotes: 1
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

16-71512177-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512177
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512177
    reference: chr 16
allele count: 1
allele frequency: 8.338336335134414e-6
allele num: 119928
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.228A>G
  hgvsp: ENST00000564230.1:c.228A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*185A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.228A>G
  hgvsp: ENST00000561908.1:c.228A>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.189A>G
  hgvsp: ENST00000561469.1:c.189A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.228A>G
  hgvsp: ENST00000568815.1:c.228A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.18A>G
  hgvsp: ENST00000565100.2:c.18A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.228A>G
  hgvsp: ENST00000288177.5:c.228A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.228A>G
  hgvsp: ENST00000567225.1:c.228A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*109A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.102A>G
  hgvsp: ENST00000565637.1:c.102A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.820A>G
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu76Glu
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

16-71512179-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512179
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512179
    reference: chr 16
allele count: 1
allele frequency: 8.337502084375522e-6
allele num: 119940
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*107G>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.226G>C
  hgvsp: ENSP00000288177.5:p.Glu76Gln
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.16G>C
  hgvsp: ENSP00000462810.1:p.Glu6Gln
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.226G>C
  hgvsp: ENSP00000463741.1:p.Glu76Gln
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.100G>C
  hgvsp: ENSP00000454864.1:p.Glu34Gln
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.818G>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.187G>C
  hgvsp: ENSP00000462021.1:p.Glu63Gln
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.226G>C
  hgvsp: ENSP00000455796.1:p.Glu76Gln
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.226G>C
  hgvsp: ENSP00000462566.1:p.Glu76Gln
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.226G>C
  hgvsp: ENSP00000458105.1:p.Glu76Gln
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*183G>C
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu76Gln
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS

16-71512179-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512179
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512179
    reference: chr 16
allele count: 1
allele frequency: 8.337502084375522e-6
allele num: 119940
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.187G>A
  hgvsp: ENSP00000462021.1:p.Glu63Lys
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.226G>A
  hgvsp: ENSP00000288177.5:p.Glu76Lys
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.16G>A
  hgvsp: ENSP00000462810.1:p.Glu6Lys
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.100G>A
  hgvsp: ENSP00000454864.1:p.Glu34Lys
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.226G>A
  hgvsp: ENSP00000463741.1:p.Glu76Lys
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.226G>A
  hgvsp: ENSP00000458105.1:p.Glu76Lys
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.226G>A
  hgvsp: ENSP00000462566.1:p.Glu76Lys
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.226G>A
  hgvsp: ENSP00000455796.1:p.Glu76Lys
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*183G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*107G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.818G>A
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42187
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu76Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/16-71512191-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512191
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512191
    reference: chr 16
allele count: 1
allele frequency: 8.338336335134414e-6
allele num: 119928
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.214G>T
  hgvsp: ENSP00000462566.1:p.Ala72Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.214G>T
  hgvsp: ENSP00000458105.1:p.Ala72Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.175G>T
  hgvsp: ENSP00000462021.1:p.Ala59Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*171G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.88G>T
  hgvsp: ENSP00000454864.1:p.Ala30Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*95G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.214G>T
  hgvsp: ENSP00000455575.1:p.Ala72Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.214G>T
  hgvsp: ENSP00000455796.1:p.Ala72Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.214G>T
  hgvsp: ENSP00000463741.1:p.Ala72Ser
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.214G>T
  hgvsp: ENSP00000288177.5:p.Ala72Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.806G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.4G>T
  hgvsp: ENSP00000462810.1:p.Ala2Ser
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41848
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala72Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD

16-71512193-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512193
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512193
    reference: chr 16
allele count: 1
allele frequency: 8.342092530490349e-6
allele num: 119874
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.212T>C
  hgvsp: ENSP00000458105.1:p.Met71Thr
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.212T>C
  hgvsp: ENSP00000463741.1:p.Met71Thr
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.212T>C
  hgvsp: ENSP00000455796.1:p.Met71Thr
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*93T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.86T>C
  hgvsp: ENSP00000454864.1:p.Met29Thr
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.212T>C
  hgvsp: ENSP00000455575.1:p.Met71Thr
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.173T>C
  hgvsp: ENSP00000462021.1:p.Met58Thr
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*169T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.212T>C
  hgvsp: ENSP00000288177.5:p.Met71Thr
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.2T>C
  hgvsp: ENSP00000462810.1:p.Met1?
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.212T>C
  hgvsp: ENSP00000462566.1:p.Met71Thr
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.804T>C
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum

16-71512194-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512194
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512194
    reference: chr 16
allele count: 2
allele frequency: 1.668724760537997e-5
allele num: 119852
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.211A>G
  hgvsp: ENSP00000455575.1:p.Met71Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.211A>G
  hgvsp: ENSP00000462566.1:p.Met71Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.85A>G
  hgvsp: ENSP00000454864.1:p.Met29Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.1A>G
  hgvsp: ENSP00000462810.1:p.Met1?
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.172A>G
  hgvsp: ENSP00000462021.1:p.Met58Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.211A>G
  hgvsp: ENSP00000463741.1:p.Met71Val
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.211A>G
  hgvsp: ENSP00000288177.5:p.Met71Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.211A>G
  hgvsp: ENSP00000455796.1:p.Met71Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*168A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*92A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.211A>G
  hgvsp: ENSP00000458105.1:p.Met71Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.803A>G
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

16-71512196-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512196
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512196
    reference: chr 16
allele count: 1
allele frequency: 8.350870160670742e-6
allele num: 119748
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.209A>G
  hgvsp: ENSP00000455575.1:p.Asp70Gly
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.209A>G
  hgvsp: ENSP00000462566.1:p.Asp70Gly
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.801A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.209A>G
  hgvsp: ENSP00000455796.1:p.Asp70Gly
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*90A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.209A>G
  hgvsp: ENSP00000288177.5:p.Asp70Gly
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*166A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.83A>G
  hgvsp: ENSP00000454864.1:p.Asp28Gly
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.209A>G
  hgvsp: ENSP00000463741.1:p.Asp70Gly
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.209A>G
  hgvsp: ENSP00000458105.1:p.Asp70Gly
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.170A>G
  hgvsp: ENSP00000462021.1:p.Asp57Gly
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-2A>G
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp70Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

16-71512197-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512197
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512197
    reference: chr 16
allele count: 1
allele frequency: 8.350730688935283e-6
allele num: 119750
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.208G>A
  hgvsp: ENSP00000288177.5:p.Asp70Asn
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*165G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.208G>A
  hgvsp: ENSP00000462566.1:p.Asp70Asn
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-3G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.208G>A
  hgvsp: ENSP00000455575.1:p.Asp70Asn
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*89G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.208G>A
  hgvsp: ENSP00000463741.1:p.Asp70Asn
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.82G>A
  hgvsp: ENSP00000454864.1:p.Asp28Asn
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.208G>A
  hgvsp: ENSP00000455796.1:p.Asp70Asn
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.800G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.169G>A
  hgvsp: ENSP00000462021.1:p.Asp57Asn
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.208G>A
  hgvsp: ENSP00000458105.1:p.Asp70Asn
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2960
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp70Asn
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

16-71512221-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512221
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512221
    reference: chr 16
allele count: 5
allele frequency: 4.252423881612519e-5
allele num: 117580
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-27C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.184C>T
  hgvsp: ENST00000564225.1:c.184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.184C>T
  hgvsp: ENST00000567225.1:c.184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*141C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.145C>T
  hgvsp: ENST00000561469.1:c.145C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.184C>T
  hgvsp: ENST00000564230.1:c.184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*65C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.184C>T
  hgvsp: ENST00000561908.1:c.184C>T(p.%3D)
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.184C>T
  hgvsp: ENST00000288177.5:c.184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.184C>T
  hgvsp: ENST00000568815.1:c.184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.776C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.58C>T
  hgvsp: ENST00000565637.1:c.58C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11403
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu62Leu
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD

16-71512227-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512227
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512227
    reference: chr 16
allele count: 1
allele frequency: 8.583543630152271e-6
allele num: 116502
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*59C>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-33C>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.178C>G
  hgvsp: ENSP00000455575.1:p.Pro60Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.139C>G
  hgvsp: ENSP00000462021.1:p.Pro47Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*135C>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.178C>G
  hgvsp: ENSP00000463741.1:p.Pro60Ala
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.178C>G
  hgvsp: ENSP00000288177.5:p.Pro60Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.178C>G
  hgvsp: ENSP00000462566.1:p.Pro60Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.178C>G
  hgvsp: ENSP00000455796.1:p.Pro60Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.178C>G
  hgvsp: ENSP00000458105.1:p.Pro60Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.52C>G
  hgvsp: ENSP00000454864.1:p.Pro18Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.770C>G
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro60Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

16-71512235-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512235
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512235
    reference: chr 16
allele count: 1
allele frequency: 8.765471056414571e-6
allele num: 114084
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.170T>C
  hgvsp: ENSP00000458105.1:p.Val57Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*51T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.170T>C
  hgvsp: ENSP00000462566.1:p.Val57Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.131T>C
  hgvsp: ENSP00000462021.1:p.Val44Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-41T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.44T>C
  hgvsp: ENSP00000454864.1:p.Val15Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*127T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.170T>C
  hgvsp: ENSP00000288177.5:p.Val57Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.170T>C
  hgvsp: ENSP00000455796.1:p.Val57Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.170T>C
  hgvsp: ENSP00000455575.1:p.Val57Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.170T>C
  hgvsp: ENSP00000463741.1:p.Val57Ala
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.762T>C
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val57Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

16-71512237-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512237
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512237
    reference: chr 16
allele count: 1
allele frequency: 8.866663120001419e-6
allele num: 112782
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.129A>C
  hgvsp: ENST00000561469.1:c.129A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.168A>C
  hgvsp: ENST00000564230.1:c.168A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.168A>C
  hgvsp: ENST00000288177.5:c.168A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*49A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.760A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.168A>C
  hgvsp: ENST00000567225.1:c.168A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.168A>C
  hgvsp: ENST00000561908.1:c.168A>C(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.168A>C
  hgvsp: ENST00000564225.1:c.168A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.168A>C
  hgvsp: ENST00000568815.1:c.168A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*125A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-43A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.42A>C
  hgvsp: ENST00000565637.1:c.42A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33735
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro56Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ

16-71512245-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512245
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512245
    reference: chr 16
allele count: 1
allele frequency: 9.202341075569625e-6
allele num: 108668
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-1G>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-1G>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-1G>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-1G>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-1G>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-1G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.752G>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-1G>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*42-1G>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-1G>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-1G>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-1G>C
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8852
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9731
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.161-1G>C
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum

16-71512247-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512247
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512247
    reference: chr 16
allele count: 1
allele frequency: 9.388966087054494e-6
allele num: 106508
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-3C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-3C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-3C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-3C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-3C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*42-3C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-3C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.750C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-3C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-3C>A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-3C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-3C>A
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7072
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10983
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.161-3C>A
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

16-71512253-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512253
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512252
    reference: chr 16
allele count: 1
allele frequency: 9.657170449058426e-6
allele num: 103550
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-10delC
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*42-10delC
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-10delC
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-10delC
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-10delC
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-10delC
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-10delC
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-10delC
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-10delC
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.743delC
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-10delC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-10delC
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: AG
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

16-71512258-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512258
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512258
    reference: chr 16
allele count: 2
allele frequency: 1.989772568995364e-5
allele num: 100514
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-14C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-14C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-14C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-14C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-14C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-14C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.739C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*42-14C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-14C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-14C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-14C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-14C>A
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

16-71512259-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512259
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512259
    reference: chr 16
allele count: 1
allele frequency: 9.978645698205839e-6
allele num: 100214
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.738T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-15T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-15T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-15T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-15T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-15T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-15T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-15T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-15T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-15T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-15T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*42-15T>C
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18048
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9613
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: A
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

16-71512264-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512264
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512264
    reference: chr 16
allele count: 2
allele frequency: 2.059732234809475e-5
allele num: 97100
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-20C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-20C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*42-20C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-20C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-20C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.733C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-20C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-20C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-20C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-20C>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-20C>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-20C>A
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10468
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12500
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS

16-71512268-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512268
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512268
    reference: chr 16
allele count: 2
allele frequency: 2.148781640809661e-5
allele num: 93076
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-24G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.729G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-24G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*42-24G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-24G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-24G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-24G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-24G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-24G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-24G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-24G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-24G>A
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5384
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8754
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23266
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

16-71512294-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512294
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512294
    reference: chr 16
allele count: 1
allele frequency: 1.416470721550186e-5
allele num: 70598
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-50T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-50T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-50T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-50T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*41+44T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.703T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-50T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-50T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-50T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-50T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-50T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-50T>C
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18909
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7488
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4020
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

16-71512342-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512342
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512342
    reference: chr 16
allele count: 1
allele frequency: 5.389673385792821e-5
allele num: 18554
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-98C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*37C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.655C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-98C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-98C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-98C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-98C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-98C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-98C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-98C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-98C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-98C>T
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33553
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8148
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

16-71512346-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512346
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512346
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 17824
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-102C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-102C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-102C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-102C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-102C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-102C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*33C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.651C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-102C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-102C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-102C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-102C>T
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7284
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33588
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-71512350-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512350
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512350
    reference: chr 16
allele count: 3
allele frequency: 1.732701859766663e-4
allele num: 17314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-106A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-106A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-106A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*29A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-106A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.647A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-106A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-106A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-106A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-106A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-106A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-106A>G
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6605
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33548
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.75e1
  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: 1123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-71512350-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512350
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512349
    reference: chr 16
allele count: 1
allele frequency: 5.775672865888876e-5
allele num: 17314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-107delG
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*28delG
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-107delG
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-107delG
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-107delG
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-107delG
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-107delG
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-107delG
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.646delG
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-107delG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-107delG
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-107delG
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33548
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: TC
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

16-71512358-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512358
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512358
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 16096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-114T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-114T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-114T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-114T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-114T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*21T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-114T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.639T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-114T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-114T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-114T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-114T>C
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5134
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32093
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

16-71512361-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512361
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512361
    reference: chr 16
allele count: 1
allele frequency: 6.254691018263698e-5
allele num: 15988
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.636T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*18T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-117T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-117T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-117T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-117T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-117T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-117T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-117T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-117T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-117T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-117T>C
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32016
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

16-71512377-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512377
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512377
    reference: chr 16
allele count: 4
allele frequency: 2.708559046587215e-4
allele num: 14768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-133C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-133C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-133C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-133C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-133C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-133C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-133C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-133C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.*2C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-133C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.620C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-133C>T
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28476
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  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: 127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/16-71512395-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512395
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512395
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 13882
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-151G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-151G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-151G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-151G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-151G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.176G>T
  hgvsp: ENSP00000454549.1:p.Cys59Phe
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.602G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-151G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-151G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-151G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-151G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-151G>T
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24507
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys59Phe
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-71512412-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512412
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512413
    reference: chr 16
allele count: 6
allele frequency: 4.723665564478035e-4
allele num: 12702
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.161-3dupT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-169dupT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-169dupT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-169dupT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-169dupT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-169dupT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.584dupT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-169dupT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-169dupT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-169dupT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-169dupT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-169dupT
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: splice region
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.161-3dupT
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS

16-71512412-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512412
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512411
    reference: chr 16
allele count: 4
allele frequency: 3.14911037631869e-4
allele num: 12702
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-169delT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-169delT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-169delT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.584delT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-169delT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-169delT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.161-3delT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-169delT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-169delT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-169delT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-169delT
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-169delT
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: splice region
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.161-3delT
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: TA
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-71512418-AAACACTCAAGG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512418
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512407
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 12960
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22489
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  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: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: AAACACTCAAGG
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/16-71512433-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512433
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512433
    reference: chr 16
allele count: 1
allele frequency: 7.937767899666614e-5
allele num: 12598
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.161-189T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.122-189T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.161-23T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.161-189T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.564T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-189T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.161-189T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.35-189T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*118-189T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.161-189T>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.161-189T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.161-189T>G
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23474
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

16-71512738-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512738
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512738
    reference: chr 16
allele count: 1
allele frequency: 8.353381448810478e-6
allele num: 119712
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.160+44G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-494G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.160+44G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.160+44G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.34+44G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.160+44G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.259G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.160+44G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.160+44G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.160+44G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.121+44G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*117+44G>A
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29991
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS

16-71512753-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512753
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512753
    reference: chr 16
allele count: 1
allele frequency: 8.324869715788949e-6
allele num: 120122
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.121+29A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.160+29A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.160+29A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.34+29A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-509A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.160+29A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.160+29A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.160+29A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.160+29A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.160+29A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*117+29A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.244A>G
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

16-71512753-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512753
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512753
    reference: chr 16
allele count: 11
allele frequency: 9.157356687367842e-5
allele num: 120122
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.160+29A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.160+29A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.160+29A>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.160+29A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*117+29A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.34+29A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.244A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.160+29A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.160+29A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-509A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.121+29A>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.160+29A>C
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

16-71512762-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512762
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512762
    reference: chr 16
allele count: 2
allele frequency: 1.658704883227176e-5
allele num: 120576
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.160+20A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-518A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.160+20A>G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.160+20A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.235A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*117+20A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.160+20A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.34+20A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.160+20A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.121+20A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.160+20A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.160+20A>G
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

16-71512763-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512763
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512763
    reference: chr 16
allele count: 1
allele frequency: 8.289949265510494e-6
allele num: 120628
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-519T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.160+19T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.34+19T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.234T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.160+19T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.160+19T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.121+19T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.160+19T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*117+19T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.160+19T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.160+19T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.160+19T>C
  variant of: http://identifiers.org/hgnc/12981
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/16-71512776-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512776
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512776
    reference: chr 16
allele count: 2
allele frequency: 1.650628063978344e-5
allele num: 121166
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.160+6G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.160+6G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*117+6G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-532G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.160+6G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.121+6G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.160+6G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.160+6G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.34+6G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.160+6G>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.160+6G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.221G>T
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.160+6G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-71512783-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512783
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512783
    reference: chr 16
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.159G>A
  hgvsp: ENST00000561908.1:c.159G>A(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.159G>A
  hgvsp: ENST00000564230.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.33G>A
  hgvsp: ENST00000565637.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.159G>A
  hgvsp: ENST00000568815.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.159G>A
  hgvsp: ENST00000564225.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.159G>A
  hgvsp: ENST00000567225.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.159G>A
  hgvsp: ENST00000288177.5:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.214G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.120G>A
  hgvsp: ENST00000561469.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*116G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.159G>A
  hgvsp: ENST00000565541.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-539G>A
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13534
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.159G>A
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ

16-71512788-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512788
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512788
    reference: chr 16
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.154G>A
  hgvsp: ENSP00000455796.1:p.Ala52Thr
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.154G>A
  hgvsp: ENSP00000462566.1:p.Ala52Thr
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.154G>A
  hgvsp: ENSP00000455575.1:p.Ala52Thr
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.154G>A
  hgvsp: ENSP00000454549.1:p.Ala52Thr
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.154G>A
  hgvsp: ENSP00000458105.1:p.Ala52Thr
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*111G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.154G>A
  hgvsp: ENSP00000463741.1:p.Ala52Thr
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.209G>A
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.28G>A
  hgvsp: ENSP00000454864.1:p.Ala10Thr
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.154G>A
  hgvsp: ENSP00000288177.5:p.Ala52Thr
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.115G>A
  hgvsp: ENSP00000462021.1:p.Ala39Thr
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-544G>A
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala52Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

16-71512790-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512790
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512790
    reference: chr 16
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.152C>G
  hgvsp: ENSP00000462566.1:p.Thr51Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.113C>G
  hgvsp: ENSP00000462021.1:p.Thr38Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.26C>G
  hgvsp: ENSP00000454864.1:p.Thr9Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.152C>G
  hgvsp: ENSP00000288177.5:p.Thr51Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.152C>G
  hgvsp: ENSP00000458105.1:p.Thr51Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.152C>G
  hgvsp: ENSP00000463741.1:p.Thr51Ser
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.152C>G
  hgvsp: ENSP00000455796.1:p.Thr51Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.152C>G
  hgvsp: ENSP00000455575.1:p.Thr51Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.152C>G
  hgvsp: ENSP00000454549.1:p.Thr51Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*109C>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-546C>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.207C>G
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr51Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

16-71512791-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512791
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512791
    reference: chr 16
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.151A>G
  hgvsp: ENSP00000455796.1:p.Thr51Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*108A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.25A>G
  hgvsp: ENSP00000454864.1:p.Thr9Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.151A>G
  hgvsp: ENSP00000455575.1:p.Thr51Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.151A>G
  hgvsp: ENSP00000288177.5:p.Thr51Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.206A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.112A>G
  hgvsp: ENSP00000462021.1:p.Thr38Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-547A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.151A>G
  hgvsp: ENSP00000463741.1:p.Thr51Ala
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.151A>G
  hgvsp: ENSP00000458105.1:p.Thr51Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.151A>G
  hgvsp: ENSP00000454549.1:p.Thr51Ala
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.151A>G
  hgvsp: ENSP00000462566.1:p.Thr51Ala
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31003
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12103
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr51Ala
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-71512792-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512792
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512792
    reference: chr 16
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.150G>T
  hgvsp: ENST00000568815.1:c.150G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.24G>T
  hgvsp: ENST00000565637.1:c.24G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.150G>T
  hgvsp: ENST00000561908.1:c.150G>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.150G>T
  hgvsp: ENST00000567225.1:c.150G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.111G>T
  hgvsp: ENST00000561469.1:c.111G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.205G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.150G>T
  hgvsp: ENST00000565541.1:c.150G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-548G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.150G>T
  hgvsp: ENST00000288177.5:c.150G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*107G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.150G>T
  hgvsp: ENST00000564225.1:c.150G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.150G>T
  hgvsp: ENST00000564230.1:c.150G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu50Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

16-71512808-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512808
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512808
    reference: chr 16
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.134A>T
  hgvsp: ENSP00000288177.5:p.Glu45Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.95A>T
  hgvsp: ENSP00000462021.1:p.Glu32Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.134A>T
  hgvsp: ENSP00000455796.1:p.Glu45Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.134A>T
  hgvsp: ENSP00000462566.1:p.Glu45Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.134A>T
  hgvsp: ENSP00000455575.1:p.Glu45Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.134A>T
  hgvsp: ENSP00000458105.1:p.Glu45Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*91A>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.189A>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.134A>T
  hgvsp: ENSP00000463741.1:p.Glu45Val
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.8A>T
  hgvsp: ENSP00000454864.1:p.Glu3Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.134A>T
  hgvsp: ENSP00000454549.1:p.Glu45Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-564A>T
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu45Val
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

16-71512812-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512812
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512812
    reference: chr 16
allele count: 4
allele frequency: 3.295001482750667e-5
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.130T>C
  hgvsp: ENST00000567225.1:c.130T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.130T>C
  hgvsp: ENST00000288177.5:c.130T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.130T>C
  hgvsp: ENST00000564230.1:c.130T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.130T>C
  hgvsp: ENST00000565541.1:c.130T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.185T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*87T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-568T>C
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.130T>C
  hgvsp: ENST00000568815.1:c.130T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.91T>C
  hgvsp: ENST00000561469.1:c.91T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.130T>C
  hgvsp: ENST00000561908.1:c.130T>C(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.130T>C
  hgvsp: ENST00000564225.1:c.130T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.4T>C
  hgvsp: ENST00000565637.1:c.4T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12083
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu44Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/16-71512819-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512819
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512819
    reference: chr 16
allele count: 5
allele frequency: 4.118616144975288e-5
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.-4T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*80T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.84T>G
  hgvsp: ENSP00000462021.1:p.Ser28Arg
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.123T>G
  hgvsp: ENSP00000463741.1:p.Ser41Arg
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.123T>G
  hgvsp: ENSP00000455796.1:p.Ser41Arg
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.123T>G
  hgvsp: ENSP00000288177.5:p.Ser41Arg
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.123T>G
  hgvsp: ENSP00000458105.1:p.Ser41Arg
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.123T>G
  hgvsp: ENSP00000455575.1:p.Ser41Arg
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.123T>G
  hgvsp: ENSP00000454549.1:p.Ser41Arg
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.123T>G
  hgvsp: ENSP00000462566.1:p.Ser41Arg
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-575T>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.178T>G
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: missense
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser41Arg
num of homozygotes: 1
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

16-71512819-A-ACTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512819
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512822
    reference: chr 16
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: ACTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-578_-50-576dupAAG
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*77_*79dupAAG
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.120_122dupAAG
  hgvsp: ENSP00000463741.1:p.Arg40dup
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.120_122dupAAG
  hgvsp: ENSP00000455796.1:p.Arg40dup
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.-7_-5dupAAG
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.120_122dupAAG
  hgvsp: ENSP00000288177.5:p.Arg40dup
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.81_83dupAAG
  hgvsp: ENSP00000462021.1:p.Arg27dup
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.120_122dupAAG
  hgvsp: ENSP00000458105.1:p.Arg40dup
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.120_122dupAAG
  hgvsp: ENSP00000455575.1:p.Arg40dup
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.175_177dupAAG
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.120_122dupAAG
  hgvsp: ENSP00000462566.1:p.Arg40dup
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.120_122dupAAG
  hgvsp: ENSP00000454549.1:p.Arg40dup
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg40dup
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

16-71512824-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512824
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512824
    reference: chr 16
allele count: 4
allele frequency: 3.29489291598023e-5
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.118A>G
  hgvsp: ENSP00000458105.1:p.Arg40Gly
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.79A>G
  hgvsp: ENSP00000462021.1:p.Arg27Gly
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.118A>G
  hgvsp: ENSP00000454549.1:p.Arg40Gly
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.173A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.-9A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.118A>G
  hgvsp: ENSP00000455575.1:p.Arg40Gly
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.118A>G
  hgvsp: ENSP00000462566.1:p.Arg40Gly
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-580A>G
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.118A>G
  hgvsp: ENSP00000455796.1:p.Arg40Gly
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.118A>G
  hgvsp: ENSP00000288177.5:p.Arg40Gly
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.118A>G
  hgvsp: ENSP00000463741.1:p.Arg40Gly
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*75A>G
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13546
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31073
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg40Gly
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

16-71512825-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512825
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512825
    reference: chr 16
allele count: 159
allele frequency: 1.30969835752294e-3
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.117C>T
  hgvsp: ENST00000561908.1:c.117C>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.-10C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.117C>T
  hgvsp: ENST00000288177.5:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*74C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.117C>T
  hgvsp: ENST00000568815.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.78C>T
  hgvsp: ENST00000561469.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.172C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-581C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.117C>T
  hgvsp: ENST00000565541.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.117C>T
  hgvsp: ENST00000564225.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.117C>T
  hgvsp: ENST00000567225.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.117C>T
  hgvsp: ENST00000564230.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13549
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 9.75e1
  variant carriers: 131
genotype quality: GenotypeQuality
hgvs: p.Tyr39Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

16-71512841-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512841
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512841
    reference: chr 16
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.101C>T
  hgvsp: ENSP00000463741.1:p.Ala34Val
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.101C>T
  hgvsp: ENSP00000454549.1:p.Ala34Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.62C>T
  hgvsp: ENSP00000462021.1:p.Ala21Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*58C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.101C>T
  hgvsp: ENSP00000462566.1:p.Ala34Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.101C>T
  hgvsp: ENSP00000455796.1:p.Ala34Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-597C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.101C>T
  hgvsp: ENSP00000455575.1:p.Ala34Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.101C>T
  hgvsp: ENSP00000458105.1:p.Ala34Val
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.-26C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.156C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.101C>T
  hgvsp: ENSP00000288177.5:p.Ala34Val
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12105
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala34Val
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-71512842-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512842
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512842
    reference: chr 16
allele count: 28
allele frequency: 2.306425041186161e-4
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*57G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.100G>T
  hgvsp: ENSP00000288177.5:p.Ala34Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.100G>T
  hgvsp: ENSP00000454549.1:p.Ala34Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.155G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.100G>T
  hgvsp: ENSP00000458105.1:p.Ala34Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.100G>T
  hgvsp: ENSP00000455796.1:p.Ala34Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.61G>T
  hgvsp: ENSP00000462021.1:p.Ala21Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.100G>T
  hgvsp: ENSP00000455575.1:p.Ala34Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.-27G>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.100G>T
  hgvsp: ENSP00000462566.1:p.Ala34Ser
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.100G>T
  hgvsp: ENSP00000463741.1:p.Ala34Ser
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-598G>T
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31146
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala34Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum

16-71512852-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71512852
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 71512852
    reference: chr 16
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157429
  ensembl transcript: ENST00000562210
  gene symbol: ZNF19
  hgvsc: ENST00000562210.1:n.145C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454549
  ensembl transcript: ENST00000565541
  gene symbol: ZNF19
  hgvsc: ENST00000565541.1:c.90C>T
  hgvsp: ENST00000565541.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462021
  ensembl transcript: ENST00000561469
  gene symbol: ZNF19
  hgvsc: ENST00000561469.1:c.51C>T
  hgvsp: ENST00000561469.1:c.51C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000288177
  ensembl transcript: ENST00000288177
  gene symbol: ZNF19
  hgvsc: ENST00000288177.5:c.90C>T
  hgvsp: ENST00000288177.5:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462810
  ensembl transcript: ENST00000565100
  gene symbol: ZNF19
  hgvsc: ENST00000565100.2:c.-50-608C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455796
  ensembl transcript: ENST00000568815
  gene symbol: ZNF19
  hgvsc: ENST00000568815.1:c.90C>T
  hgvsp: ENST00000568815.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000261611
  ensembl protein: ENSP00000463741
  ensembl transcript: ENST00000561908
  gene symbol: AC010547.9
  hgvsc: ENST00000561908.1:c.90C>T
  hgvsp: ENST00000561908.1:c.90C>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000462566
  ensembl transcript: ENST00000567225
  gene symbol: ZNF19
  hgvsc: ENST00000567225.1:c.90C>T
  hgvsp: ENST00000567225.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000458105
  ensembl transcript: ENST00000564230
  gene symbol: ZNF19
  hgvsc: ENST00000564230.1:c.90C>T
  hgvsp: ENST00000564230.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000455575
  ensembl transcript: ENST00000564225
  gene symbol: ZNF19
  hgvsc: ENST00000564225.1:c.90C>T
  hgvsp: ENST00000564225.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000454864
  ensembl transcript: ENST00000565637
  gene symbol: ZNF19
  hgvsc: ENST00000565637.1:c.-37C>T
  variant of: http://identifiers.org/hgnc/12981
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157429
  ensembl protein: ENSP00000456143
  ensembl transcript: ENST00000569717
  gene symbol: ZNF19
  hgvsc: ENST00000569717.1:c.*47C>T
  variant of: http://identifiers.org/hgnc/12981
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31143
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly30Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

16-71512856-G-GT
type: Variant
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: GT
canonical: true
consequence: frameshift
filter: PASS
hgvs: p.Thr29AsnfsTer52
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 473
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13205
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1967
bin: 9.75e1
variant carriers: 64

GenotypeQuality
all individuals: 4652
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1754
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1026
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5355
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16804
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7480
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8294
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 55
allele frequency: 1.020029673590504e-2
allele num: 5392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6850
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13032
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.862351529197533e-4
allele num: 48326
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.42e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.99e0

DP
type: SiteQuality
SIO_000300: 1.029066e6

FS
type: SiteQuality
SIO_000300: 6.870000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.85e-1

GenotypeQuality
all individuals: 2078
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4509
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4452
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 881
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1427
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13383
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1905
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 655
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19582
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6874
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6884
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.195600191296031e-4
allele num: 8364
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13048
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5418
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 706
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48692
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.379e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.37e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.327e0

DP
type: SiteQuality
SIO_000300: 1.058645e6

GenotypeQuality
all individuals: 208
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5229
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25479
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3718
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2892
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12851
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1910
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 232
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 901
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2416
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50164
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7100
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8712
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5524
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.505e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.12375e6

QD
type: SiteQuality
SIO_000300: 1.416e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

VQSLOD
type: SiteQuality
SIO_000300: -9.903999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.094e0

GenotypeQuality
all individuals: 438
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27724
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4557
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2398
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2546
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12392
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8908
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 1.042632066728452e-3
allele num: 8632
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5584
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.963710627601917e-5
allele num: 50924
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.371e1

VQSLOD
type: SiteQuality
SIO_000300: 3.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.16e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.150275e6

GenotypeQuality
all individuals: 676
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1973
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2659
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3883
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30384
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11682
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1912
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 353
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 777
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2948
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.759705103098721e-5
allele num: 52086
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9146
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8700
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13598
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7340
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.367e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.45e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.45e-1

DP
type: SiteQuality
SIO_000300: 1.180639e6

VQSLOD
type: SiteQuality
SIO_000300: 3.77e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

GenotypeQuality
all individuals: 3454
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11132
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1735
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.5e0
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 562
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31701
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2736
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1911
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 298
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.316359379572725e-5
allele num: 13668
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52930
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7418
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8760
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5718
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9284
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.899e1

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.200334e6

VQSLOD
type: SiteQuality
SIO_000300: 1.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.77e-1

QD
type: SiteQuality
SIO_000300: 1.226e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.89e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.29e-1

FS
type: SiteQuality
SIO_000300: 2.435e0

GenotypeQuality
all individuals: 10813
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 569
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2590
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5736
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.338688085676038e-4
allele num: 7470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53340
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9376
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8806
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13762
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.907e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.976e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e0

DP
type: SiteQuality
SIO_000300: 1.210684e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

QD
type: SiteQuality
SIO_000300: 2.048e1

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 684
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variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2035
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.400734499891985e-5
allele num: 55548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14042
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5874
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8954
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7718
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.52e-1

QD
type: SiteQuality
SIO_000300: 9.93e0

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.231e0

DP
type: SiteQuality
SIO_000300: 1.259749e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.043e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.22e-1

GenotypeDepth
all individuals: 162
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 102
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4324
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3497
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1920
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variant carriers: 1

GenotypeQuality
all individuals: 243
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variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44819
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variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
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variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
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variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15008
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6260
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 9.386146048432514e-5
allele num: 10654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62244
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.53e-1

QD
type: SiteQuality
SIO_000300: 2.217e1

VQSLOD
type: SiteQuality
SIO_000300: -1.724e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.6e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.61e-1

DP
type: SiteQuality
SIO_000300: 1.386593e6

MQ
type: SiteQuality
SIO_000300: 5.901e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

GenotypeDepth
all individuals: 429
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2327
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 912
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variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 378
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variant carriers: 0

GenotypeQuality
all individuals: 402
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variant carriers: 0

GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 113
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 5.25e1
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GenotypeQuality
all individuals: 3727
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
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variant carriers: 1

GenotypeQuality
all individuals: 47866
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64676
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.054690329590728e-5
allele num: 11044
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6450
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15492
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.184e0

QD
type: SiteQuality
SIO_000300: 1.257e1

FS
type: SiteQuality
SIO_000300: 1.7591e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.586e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 1.432732e6

MQRankSum
type: SiteQuality
SIO_000300: -1.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeDepth
all individuals: 209
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 246
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variant carriers: 0

GenotypeQuality
all individuals: 353
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variant carriers: 0

GenotypeQuality
all individuals: 148
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GenotypeQuality
all individuals: 236
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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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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 879
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48180
bin: 6.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6460
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.542257865515114e-5
allele num: 64840
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15538
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11078
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

VQSLOD
type: SiteQuality
SIO_000300: 5.32e-1

MQ
type: SiteQuality
SIO_000300: 5.883e1

DP
type: SiteQuality
SIO_000300: 1.437144e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.92e-1

FS
type: SiteQuality
SIO_000300: 3.095e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.93e-1

QD
type: SiteQuality
SIO_000300: 1.177e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.152e0

GenotypeDepth
all individuals: 65
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
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variant carriers: 0

GenotypeQuality
all individuals: 239
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GenotypeQuality
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GenotypeQuality
all individuals: 139
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GenotypeQuality
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GenotypeQuality
all individuals: 5
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GenotypeQuality
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GenotypeQuality
all individuals: 16
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 246
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GenotypeQuality
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GenotypeQuality
all individuals: 309
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GenotypeQuality
all individuals: 1922
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variant carriers: 1

GenotypeQuality
all individuals: 3807
bin: 6.75e1
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GenotypeQuality
all individuals: 103
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9922
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65346
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.928571428571429e-5
allele num: 11200
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15684
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.191e0

FS
type: SiteQuality
SIO_000300: 7.404e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.17e-1

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 7.5e0

MQ
type: SiteQuality
SIO_000300: 5.787e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

DP
type: SiteQuality
SIO_000300: 1.446646e6

MQRankSum
type: SiteQuality
SIO_000300: -2.359e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 1075
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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
all individuals: 8
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GenotypeQuality
all individuals: 153
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GenotypeQuality
all individuals: 244
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GenotypeQuality
all individuals: 4
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GenotypeQuality
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GenotypeQuality
all individuals: 962
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 919
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GenotypeQuality
all individuals: 310
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GenotypeQuality
all individuals: 1921
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variant carriers: 2

GenotypeQuality
all individuals: 120
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 179
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515105602860519e-5
allele num: 66002
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.255473539346929e-5
allele num: 15986
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11332
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.1e-1

QD
type: SiteQuality
SIO_000300: 1.262e1

VQSLOD
type: SiteQuality
SIO_000300: 8.110000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.464233e6

MQ
type: SiteQuality
SIO_000300: 5.927e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 210
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 5.25e1
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GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
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GenotypeQuality
all individuals: 70
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variant carriers: 0

GenotypeQuality
all individuals: 104
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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: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 929
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.023523009010099e-5
allele num: 66148
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16054
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 6.51e0

DP
type: SiteQuality
SIO_000300: 1.469221e6

MQ
type: SiteQuality
SIO_000300: 5.905e1

MQRankSum
type: SiteQuality
SIO_000300: -1.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.366e0

FS
type: SiteQuality
SIO_000300: 1.414e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.36e0

GenotypeDepth
all individuals: 324
bin: 5.25e1
variant carriers: 14

GenotypeQuality
all individuals: 245
bin: 8.75e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 126

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 50039
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GenotypeQuality
all individuals: 308
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 78
allele frequency: 4.853764779091474e-3
allele num: 16070
num of homozygotes: 1

Latino
type: Population
allele count: 3
allele frequency: 2.636203866432338e-4
allele num: 11380
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.242152466367713e-3
allele num: 892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 43
allele frequency: 6.498806033310159e-4
allele num: 66166
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.852216748768474e-5
allele num: 10150
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.126e0

DP
type: SiteQuality
SIO_000300: 1.473017e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.25e-1

QD
type: SiteQuality
SIO_000300: 1.264e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.81e-1

GenotypeDepth
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bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 628
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variant carriers: 0

GenotypeQuality
all individuals: 93
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variant carriers: 0

GenotypeQuality
all individuals: 3977
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 900
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 1
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GenotypeQuality
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GenotypeQuality
all individuals: 80
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GenotypeQuality
all individuals: 247
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GenotypeQuality
all individuals: 938
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variant carriers: 0

GenotypeQuality
all individuals: 125
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variant carriers: 0

GenotypeQuality
all individuals: 1927
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variant carriers: 1

GenotypeQuality
all individuals: 310
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 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: 11390
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16084
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510710940568632e-5
allele num: 66194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.133e1

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

FS
type: SiteQuality
SIO_000300: 1.3017e1

DP
type: SiteQuality
SIO_000300: 1.470279e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 8.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.4e-2

MQ
type: SiteQuality
SIO_000300: 5.971e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.32e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.752e0

GenotypeDepth
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 968
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variant carriers: 0

GenotypeQuality
all individuals: 109
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variant carriers: 0

GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1927
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variant carriers: 1

GenotypeQuality
all individuals: 91
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GenotypeQuality
all individuals: 103
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GenotypeQuality
all individuals: 936
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 100
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 248
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variant carriers: 0

GenotypeQuality
all individuals: 3978
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
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variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.220452848967405e-5
allele num: 16076
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66200
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 8.720000000000001e0

DP
type: SiteQuality
SIO_000300: 1.470835e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.935e1

VQSLOD
type: SiteQuality
SIO_000300: -3.241e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: 4.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 91
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66200
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.220452848967405e-5
allele num: 16076
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
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: 10160
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e0

MQRankSum
type: SiteQuality
SIO_000300: 4.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.935e1

BaseQRankSum
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SIO_000300: 1.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.63e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.241e-1

DP
type: SiteQuality
SIO_000300: 1.470835e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
all individuals: 310
bin: 9.25e1
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GenotypeQuality
all individuals: 1925
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66162
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.222000995520159e-5
allele num: 16072
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.526e0

FS
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
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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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QD
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SIO_000300: 9.16e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 48
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GenotypeQuality
all individuals: 925
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GenotypeQuality
all individuals: 309
bin: 9.25e1
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GenotypeQuality
all individuals: 2
bin: 2.5e0
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GenotypeQuality
all individuals: 247
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GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1924
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GenotypeQuality
all individuals: 947
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GenotypeQuality
all individuals: 3981
bin: 6.75e1
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GenotypeQuality
all individuals: 50054
bin: 6.25e1
variant carriers: 0

Latino
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allele count: 0
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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African
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Other
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South Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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FS
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MQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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Other
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East Asian
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European (Non-Finnish)
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African
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
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MQRankSum
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MQ
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FS
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ReadPosRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.513500423780119e-5
allele num: 66072
num of homozygotes: 0

Latino
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African
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South Asian
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East Asian
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Other
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European (Finnish)
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MQ
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FS
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DP
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MQRankSum
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BaseQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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SIO_000300: -9.320000000000001e-1

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

African
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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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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.513500423780119e-5
allele num: 66072
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6572
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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FS
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MQ
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ClippingRankSum
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MQRankSum
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QD
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InbreedingCoeff
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 3.020539669754329e-4
allele num: 9932
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 1.797268152408339e-4
allele num: 11128
num of homozygotes: 0

European (Finnish)
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South Asian
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East Asian
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MQRankSum
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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DP
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BaseQRankSum
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MQ
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FS
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.556226462074761e-5
allele num: 64258
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61854
num of homozygotes: 0

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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num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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num of homozygotes: 0

South Asian
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allele frequency: 6.614631565021828e-5
allele num: 15118
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: -1.1e-3

ClippingRankSum
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ReadPosRankSum
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FS
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DP
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VQSLOD
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BaseQRankSum
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QD
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MQRankSum
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SIO_000300: -3.87e-1

MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Finnish)
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allele count: 1
allele frequency: 1.640419947506562e-4
allele num: 6096
num of homozygotes: 0

Other
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African
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allele count: 0
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Latino
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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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East Asian
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South Asian
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FS
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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DP
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MQ
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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South Asian
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Other
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Latino
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African
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East Asian
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FS
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ReadPosRankSum
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VQSLOD
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MQ
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DP
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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SIO_000300: -2.1e-3

QD
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GenotypeDepth
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variant carriers: 0

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

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

Other
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.783803068141277e-5
allele num: 56060
num of homozygotes: 0

European (Finnish)
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allele count: 0
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MQ
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SIO_000300: 6.036e1

ReadPosRankSum
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SIO_000300: 0.0e0

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

Other
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allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 3.682563063892469e-5
allele num: 54310
num of homozygotes: 0

European (Finnish)
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African
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Latino
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East Asian
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InbreedingCoeff
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MQRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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QD
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
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allele num: 54134
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5428
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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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8340
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 4.015580452154359e-5
allele num: 49806
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.74e-1

ClippingRankSum
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SIO_000300: -5.46e-1

VQSLOD
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BaseQRankSum
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SIO_000300: -2.477e0

MQ
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FS
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DP
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SIO_000300: 9.88887e5

QD
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SIO_000300: 1.625e1

InbreedingCoeff
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SIO_000300: -7.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6680
num of homozygotes: 0

South Asian
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allele frequency: 8.348639171814995e-5
allele num: 11978
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -6.875e-1

MQRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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SIO_000300: 5.871e1

FS
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SIO_000300: 0.0e0

DP
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SIO_000300: 8.54473e5

ClippingRankSum
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SIO_000300: -3.11e-1

QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 438
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 7610
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.628664495114007e-3
allele num: 614
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South Asian
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Other
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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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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
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SIO_000300: 1.768e1

BaseQRankSum
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SIO_000300: -1.589e0

ReadPosRankSum
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FS
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SIO_000300: 0.0e0

MQRankSum
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SIO_000300: -5.659999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.389999999999999e-2

DP
type: SiteQuality
SIO_000300: 3.60127e5

VQSLOD
type: SiteQuality
SIO_000300: -1.76e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5628
bin: 2.25e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1448
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

DP
type: SiteQuality
SIO_000300: 3.47839e5

MQRankSum
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SIO_000300: 7.31e-1

MQ
type: SiteQuality
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ClippingRankSum
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SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 1.095e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.61e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7858
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.365541327124563e-4
allele num: 6872
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.69e-2

FS
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MQRankSum
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MQ
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DP
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BaseQRankSum
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SIO_000300: 5.83e-1

QD
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VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.33e-1

ReadPosRankSum
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SIO_000300: 6.33e-1

GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6872
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
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 5.494505494505495e-3
allele num: 182
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 6080
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African
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Latino
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Other
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MQRankSum
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VQSLOD
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DP
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FS
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Other
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 1.286670097786928e-4
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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FS
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InbreedingCoeff
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MQ
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DP
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ReadPosRankSum
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SIO_000300: 2.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.05e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.869e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.233e0

QD
type: SiteQuality
SIO_000300: 1.096e1

VQSLOD
type: SiteQuality
SIO_000300: -3.737e0

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

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 3.75e1
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GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 1.25e1
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GenotypeQuality
all individuals: 25716
bin: 7.5e0
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 80
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.590132827324478e-4
allele num: 5270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7690
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 948
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.25e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

DP
type: SiteQuality
SIO_000300: 2.76436e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

QD
type: SiteQuality
SIO_000300: 1.028e1

GenotypeDepth
all individuals: 2741
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
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GenotypeQuality
all individuals: 341
bin: 7.75e1
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GenotypeQuality
all individuals: 219
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GenotypeQuality
all individuals: 10
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GenotypeQuality
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GenotypeQuality
all individuals: 25
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3686
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variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 9.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4658
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7642
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 264
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.92e-1

DP
type: SiteQuality
SIO_000300: 2.52117e5

BaseQRankSum
type: SiteQuality
SIO_000300: -5.92e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.981e1

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.24e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.54e-1

GenotypeDepth
all individuals: 1082
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 18345
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1716
bin: 2.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 69
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variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 8.079719903043361e-4
allele num: 7426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 138
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3972
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.850000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 2.40964e5

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

QD
type: SiteQuality
SIO_000300: 3.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.55e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 9.31e-1

GenotypeDepth
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
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variant carriers: 2

GenotypeQuality
all individuals: 18345
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1716
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
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variant carriers: 0

GenotypeQuality
all individuals: 69
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variant carriers: 0

GenotypeQuality
all individuals: 3308
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 236
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 165
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GenotypeQuality
all individuals: 81
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 799
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variant carriers: 1

GenotypeQuality
all individuals: 281
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.34661998384056e-4
allele num: 7426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.517623363544814e-4
allele num: 3972
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.154574132492113e-3
allele num: 634
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 138
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

FS
type: SiteQuality
SIO_000300: 9.31e-1

DP
type: SiteQuality
SIO_000300: 2.40964e5

QD
type: SiteQuality
SIO_000300: 3.76e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.850000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.78e-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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 59
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GenotypeQuality
all individuals: 846
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4108
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 240
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 138
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7534
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.065e1

DP
type: SiteQuality
SIO_000300: 2.33428e5

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.38e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 1.65e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2820
bin: 6.25e1
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GenotypeQuality
all individuals: 289
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 282
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3904
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.341201716738197e-4
allele num: 7456
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 584
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.03e1

MQ
type: SiteQuality
SIO_000300: 5.934e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.007e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.53e-2

DP
type: SiteQuality
SIO_000300: 2.23345e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e0

MQRankSum
type: SiteQuality
SIO_000300: 7.43e-1

FS
type: SiteQuality
SIO_000300: 6.412e0

VQSLOD
type: SiteQuality
SIO_000300: -1.886e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.515e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 50
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GenotypeQuality
all individuals: 823
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 747
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GenotypeQuality
all individuals: 200
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508204633204633e-5
allele num: 66304
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15302
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: -1.501e0

QD
type: SiteQuality
SIO_000300: 1.429e1

VQSLOD
type: SiteQuality
SIO_000300: -1.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.029e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.335e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.709646e6

FS
type: SiteQuality
SIO_000300: 1.1595e1

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

GenotypeQuality
all individuals: 14
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variant carriers: 0

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

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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 1.156336725254394e-4
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 9.071666162685213e-4
allele num: 6614
num of homozygotes: 0

East Asian
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African
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South Asian
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Latino
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European (Non-Finnish)
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allele frequency: 7.530120481927712e-5
allele num: 66400
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Other
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InbreedingCoeff
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BaseQRankSum
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MQ
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DP
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VQSLOD
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FS
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

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

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

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

European (Finnish)
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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DP
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MQ
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FS
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ReadPosRankSum
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SIO_000300: -4.02e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66502
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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Other
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East Asian
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allele num: 8648
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
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SIO_000300: 6.22e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66648
num of homozygotes: 0

East Asian
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allele num: 8652
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African
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num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

Other
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South Asian
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Latino
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num of homozygotes: 0

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

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

South Asian
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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African
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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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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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InbreedingCoeff
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BaseQRankSum
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QD
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

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

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

Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

QD
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BaseQRankSum
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SIO_000300: 5.620000000000001e-1

InbreedingCoeff
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SIO_000300: 1.0e-4

FS
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SIO_000300: 2.819e0

ReadPosRankSum
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DP
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ClippingRankSum
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MQ
type: SiteQuality
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VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

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

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

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

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

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

Other
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.326e1

DP
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: -2.0e-3

InbreedingCoeff
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SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 4.191e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.44e-1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
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allele num: 66704
num of homozygotes: 0

East Asian
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num of homozygotes: 0

South Asian
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Other
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.148e0

QD
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.918e1

DP
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.6e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
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allele num: 66724
num of homozygotes: 0

East Asian
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num of homozygotes: 0

South Asian
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BaseQRankSum
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SIO_000300: -1.995e0

ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 1.2321e1

DP
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MQRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 5.961e1

VQSLOD
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SIO_000300: -1.531e0

QD
type: SiteQuality
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ClippingRankSum
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SIO_000300: -5.49e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 4

GenotypeDepth
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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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

Latino
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allele frequency: 3.454828122300915e-4
allele num: 11578
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
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MQ
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InbreedingCoeff
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VQSLOD
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DP
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FS
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ClippingRankSum
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ReadPosRankSum
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QD
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MQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele num: 16512
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African
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Other
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Latino
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European (Non-Finnish)
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European (Finnish)
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BaseQRankSum
type: SiteQuality
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FS
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DP
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InbreedingCoeff
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VQSLOD
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MQRankSum
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QD
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ReadPosRankSum
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MQ
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

European (Finnish)
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num of homozygotes: 0

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

GenotypeDepth
all individuals: 78
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variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 8.25e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 1365
bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44625
bin: 6.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 216
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2012
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1867
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.422480620155039e-4
allele num: 16512
num of homozygotes: 0

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

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.54e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

DP
type: SiteQuality
SIO_000300: 1.748975e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.610000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.315e1

FS
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.773e0

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

GenotypeDepth
all individuals: 572
bin: 4.25e1
variant carriers: 3

GenotypeDepth
all individuals: 64
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 69
bin: 6.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9668
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

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

GenotypeQuality
all individuals: 1865
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variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2009
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1376
bin: 9.75e1
variant carriers: 159

GenotypeQuality
all individuals: 44622
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 8
allele frequency: 6.909656244601831e-4
allele num: 11578
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.994305409860632e-5
allele num: 66730
num of homozygotes: 0

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

African
type: Population
allele count: 143
allele frequency: 1.374207188160676e-2
allele num: 10406
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.750289e6

QD
type: SiteQuality
SIO_000300: 1.342e1

VQSLOD
type: SiteQuality
SIO_000300: 6.16e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.966e0

GenotypeDepth
all individuals: 71
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 274
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variant carriers: 1

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
all individuals: 3
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variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 721
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variant carriers: 0

GenotypeQuality
all individuals: 44745
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variant carriers: 0

GenotypeQuality
all individuals: 9689
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 201
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1872
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2010
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variant carriers: 0

GenotypeQuality
all individuals: 1226
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 216
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.731719e6

QD
type: SiteQuality
SIO_000300: 1.407e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.91e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.879999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

FS
type: SiteQuality
SIO_000300: 2.274e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -8.755000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.8e-2

GenotypeDepth
all individuals: 65
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 284
bin: 9.75e1
variant carriers: 22

GenotypeDepth
all individuals: 124
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 44740
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1872
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 720
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 201
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variant carriers: 0

GenotypeQuality
all individuals: 2009
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GenotypeQuality
all individuals: 9684
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variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1238
bin: 9.75e1
variant carriers: 28

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 216
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 28
allele frequency: 4.195762280097102e-4
allele num: 66734
num of homozygotes: 0

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.02e-1

QD
type: SiteQuality
SIO_000300: 1.379e1

DP
type: SiteQuality
SIO_000300: 1.732735e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.93e0

GenotypeDepth
all individuals: 262
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 46
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
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variant carriers: 0

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

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
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GenotypeQuality
all individuals: 44748
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2011
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1872
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9686
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 721
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1210
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 201
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.730209e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.752e0

VQSLOD
type: SiteQuality
SIO_000300: -3.529e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 6.828e0

QD
type: SiteQuality
SIO_000300: 1.317e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e-1

MQ
type: SiteQuality
SIO_000300: 5.921e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.35e-1