19-53456168-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456168
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456168
    reference: chr 19
allele count: 1
allele frequency: 8.433694295449179e-6
allele num: 118572
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-38C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-38C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-38C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-38C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-38C>G
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-38C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-38C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-55C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.170-38C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-38C>G
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9534
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3431
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

19-53456173-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456173
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456173
    reference: chr 19
allele count: 1
allele frequency: 8.448657508321927e-6
allele num: 118362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-43C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-43C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-43C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-43C>T
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.170-43C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-43C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-43C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-43C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-60C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-43C>T
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3275
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

19-53456179-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456179
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456179
    reference: chr 19
allele count: 15
allele frequency: 1.270088567509441e-4
allele num: 118102
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-49A>G
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-49A>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-49A>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-49A>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-49A>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-49A>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.170-49A>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-49A>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-66A>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-49A>G
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4838
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7893
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6125
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1800
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26554
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3436
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/19-53456490-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456490
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456491
    reference: chr 19
allele count: 943
allele frequency: 4.724448897795591e-1
allele num: 1996
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-361dupT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-361dupT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-361dupT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-361dupT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-361dupT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-361dupT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-361dupT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-361dupT
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.169+46dupT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-378dupT
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 1.25e1
  variant carriers: 824
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 2.5e0
  variant carriers: 243
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 7.5e0
  variant carriers: 1420
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 8.25e1
  variant carriers: 100
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 5.75e1
  variant carriers: 120
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 7.75e1
  variant carriers: 51
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 6.25e1
  variant carriers: 229
num of homozygotes: 77
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/19-53456490-C-CAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456490
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456492
    reference: chr 19
allele count: 52
allele frequency: 2.605210420841683e-2
allele num: 1996
alternate allele: CAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-362_64-361dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-362_64-361dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.169+45_169+46dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-362_64-361dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-362_64-361dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-379_64-378dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-362_64-361dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-362_64-361dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-362_64-361dupTT
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-362_64-361dupTT
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 7.5e0
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 2.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 1.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 2.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 6.25e1
  variant carriers: 11
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS

http://identifiers.org/exac.variant/19-53456490-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456490
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456489
    reference: chr 19
allele count: 8
allele frequency: 4.008016032064128e-3
allele num: 1996
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-361delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-361delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-361delT
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-361delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-361delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-361delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.169+46delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-361delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-361delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-378delT
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2771
  bin: 2.5e0
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: CA
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/19-53456501-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456501
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456501
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 3944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-371G>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-371G>T
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-388G>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-371G>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-371G>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-371G>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.169+36G>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-371G>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-371G>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-371G>T
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2441
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1962
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP

19-53456553-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456553
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456553
    reference: chr 19
allele count: 2
allele frequency: 2.331545814875262e-4
allele num: 8578
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-440G>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-423G>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-423G>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-423G>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.153G>A
  hgvsp: ENST00000332302.8:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-423G>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-423G>A
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-423G>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-423G>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-423G>A
  variant of: http://identifiers.org/hgnc/26995
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser51Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS

19-53456590-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456590
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456590
    reference: chr 19
allele count: 1
allele frequency: 1.016260162601626e-4
allele num: 9840
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-460C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-460C>T
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-460C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-460C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-460C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-460C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.116C>T
  hgvsp: ENSP00000333199.8:p.Ser39Leu
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-460C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-460C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-477C>T
  variant of: http://identifiers.org/hgnc/26995
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1537
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser39Leu
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-53456597-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456597
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456597
    reference: chr 19
allele count: 1
allele frequency: 1.016260162601626e-4
allele num: 9840
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-467C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-467C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-467C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-467C>A
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-467C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.109C>A
  hgvsp: ENSP00000333199.8:p.Leu37Ile
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-467C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-467C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-467C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-484C>A
  variant of: http://identifiers.org/hgnc/26995
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu37Ile
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: G
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

19-53456600-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456600
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456600
    reference: chr 19
allele count: 1
allele frequency: 1.019575856443719e-4
allele num: 9808
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-470G>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-470G>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-470G>C
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-470G>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.106G>C
  hgvsp: ENSP00000333199.8:p.Asp36His
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-487G>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-470G>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-470G>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-470G>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-470G>C
  variant of: http://identifiers.org/hgnc/26995
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 2.25e1
  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: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp36His
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS

19-53456601-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456601
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456601
    reference: chr 19
allele count: 1
allele frequency: 1.018744906275469e-4
allele num: 9816
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-471C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-471C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-471C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.105C>T
  hgvsp: ENST00000332302.8:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-471C>T
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-488C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-471C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-471C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-471C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-471C>T
  variant of: http://identifiers.org/hgnc/26995
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His35His
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

19-53456610-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456610
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456610
    reference: chr 19
allele count: 4
allele frequency: 4.080799836768007e-4
allele num: 9802
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-480G>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-480G>A
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-480G>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-480G>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-480G>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.96G>A
  hgvsp: ENST00000332302.8:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-480G>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-480G>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-497G>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-480G>A
  variant of: http://identifiers.org/hgnc/26995
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val32Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

19-53456634-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456634
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456634
    reference: chr 19
allele count: 1
allele frequency: 1.148633126579371e-4
allele num: 8706
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-504C>G
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-504C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-504C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-504C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.72C>G
  hgvsp: ENST00000332302.8:c.72C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-504C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-504C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-504C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-504C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-521C>G
  variant of: http://identifiers.org/hgnc/26995
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser24Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/19-53456645-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456645
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456646
    reference: chr 19
allele count: 149
allele frequency: 1.037604456824513e-1
allele num: 1436
alternate allele: CA
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-516dupT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-516dupT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-516dupT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-533dupT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-516dupT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-516dupT
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-516dupT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.64-4dupT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-516dupT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-516dupT
  variant of: http://identifiers.org/hgnc/26995
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 7.5e0
  variant carriers: 166
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 2.5e0
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 1.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 1.25e1
  variant carriers: 130
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2756
  bin: 2.5e0
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 7.5e0
  variant carriers: 19
hgvs: c.64-4dupT
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-53456645-C-CAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456645
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456647
    reference: chr 19
allele count: 239
allele frequency: 1.664345403899722e-1
allele num: 1436
alternate allele: CAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-517_64-516dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.64-5_64-4dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-517_64-516dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-534_64-533dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-517_64-516dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-517_64-516dupTT
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-517_64-516dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-517_64-516dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-517_64-516dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-517_64-516dupTT
  variant of: http://identifiers.org/hgnc/26995
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 2.5e0
  variant carriers: 155
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 1.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 7.5e0
  variant carriers: 542
genotype depth: GenotypeDepth
  all individuals: 0
  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: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 1.25e1
  variant carriers: 211
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 6.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 9.25e1
  variant carriers: 33
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 8.75e1
  variant carriers: 27
hgvs: c.64-5_64-4dupTT
num of homozygotes: 15
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-53456645-C-CAAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456645
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456648
    reference: chr 19
allele count: 1
allele frequency: 6.963788300835655e-4
allele num: 1436
alternate allele: CAAA
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-518_64-516dupTTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-518_64-516dupTTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-518_64-516dupTTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-518_64-516dupTTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-518_64-516dupTTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.64-6_64-4dupTTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-518_64-516dupTTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-518_64-516dupTTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-518_64-516dupTTT
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-535_64-533dupTTT
  variant of: http://identifiers.org/hgnc/26995
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
hgvs: c.64-6_64-4dupTTT
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/19-53456645-C-CAAAAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456645
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456650
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 1436
alternate allele: CAAAAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-520_64-516dupTTTTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-520_64-516dupTTTTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.64-8_64-4dupTTTTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-520_64-516dupTTTTT
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-520_64-516dupTTTTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-520_64-516dupTTTTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-537_64-533dupTTTTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-520_64-516dupTTTTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-520_64-516dupTTTTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-520_64-516dupTTTTT
  variant of: http://identifiers.org/hgnc/26995
canonical: false
consequence: splice region
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.75e1
  variant carriers: 0
hgvs: c.64-8_64-4dupTTTTT
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/19-53456645-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456645
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456644
    reference: chr 19
allele count: 110
allele frequency: 7.66016713091922e-2
allele num: 1436
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-516delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-516delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-516delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.64-4delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-516delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-516delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-516delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-516delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-533delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-516delT
  variant of: http://identifiers.org/hgnc/13827
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 7.5e0
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 1.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 1.25e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 2.25e1
  variant carriers: 10
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 quality: GenotypeQuality
  all individuals: 252
  bin: 1.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2756
  bin: 2.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 19
hgvs: c.64-4delT
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: CA
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

19-53456657-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456657
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456657
    reference: chr 19
allele count: 8
allele frequency: 4.61361014994233e-3
allele num: 1734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-527C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.64-15C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-527C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-527C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-527C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-527C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-527C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-544C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-527C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-527C>T
  variant of: http://identifiers.org/hgnc/13827
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 2.5e0
  variant carriers: 3
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: 1838
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

19-53456657-G-GAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456657
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456659
    reference: chr 19
allele count: 3
allele frequency: 1.730103806228374e-3
allele num: 1734
alternate allele: GAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-529_64-528dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-529_64-528dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-546_64-545dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-529_64-528dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-529_64-528dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-529_64-528dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.64-17_64-16dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-529_64-528dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-529_64-528dupTT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-529_64-528dupTT
  variant of: http://identifiers.org/hgnc/13827
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 2.5e0
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1072
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 1.75e1
  variant carriers: 5
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

19-53456657-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456657
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456656
    reference: chr 19
allele count: 1
allele frequency: 5.767012687427913e-4
allele num: 1734
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-528delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-528delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-545delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-528delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-528delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.64-16delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-528delT
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-528delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-528delT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-528delT
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: GA
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS

19-53456658-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456658
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456659
    reference: chr 19
allele count: 8
allele frequency: 2.434570906877663e-3
allele num: 3286
alternate allele: AG
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-529_64-528insC
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-529_64-528insC
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-529_64-528insC
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.64-17_64-16insC
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-529_64-528insC
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-529_64-528insC
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-529_64-528insC
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-529_64-528insC
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-529_64-528insC
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-546_64-545insC
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

19-53456664-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456664
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456664
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 2386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-534T>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-534T>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.64-22T>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-534T>A
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-534T>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-534T>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-534T>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-551T>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-534T>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-534T>A
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

19-53456665-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456665
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456664
    reference: chr 19
allele count: 3
allele frequency: 1.492537313432836e-3
allele num: 2010
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-536delA
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-536delA
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-536delA
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.64-24delA
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-553delA
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-536delA
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-536delA
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-536delA
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-536delA
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-536delA
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: AT
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

19-53456666-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456666
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456666
    reference: chr 19
allele count: 80
allele frequency: 5.056890012642225e-2
allele num: 1582
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-536A>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-536A>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-536A>T
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-536A>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-536A>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-536A>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-536A>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-553A>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-536A>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.64-24A>T
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 1.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 7.5e0
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 2.5e0
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 1.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 10
num of homozygotes: 2
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

19-53456667-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456667
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456667
    reference: chr 19
allele count: 1
allele frequency: 5.662514156285391e-4
allele num: 1766
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-537T>C
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-537T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-537T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-554T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-537T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-537T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.64-25T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-537T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-537T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-537T>C
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1487
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD

19-53456686-CAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53456686
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53456684
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 308
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.64-558_64-557delAT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.64-558_64-557delAT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.64-46_64-45delAT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.64-558_64-557delAT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.64-558_64-557delAT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.64-558_64-557delAT
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.64-575_64-574delAT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.64-558_64-557delAT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.64-558_64-557delAT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.64-558_64-557delAT
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1044
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: CAT
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

19-53459230-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459230
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459230
    reference: chr 19
allele count: 17
allele frequency: 1.420430808308685e-4
allele num: 119682
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.63+50G>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.63+50G>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.63+50G>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.63+50G>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.63+50G>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.63+50G>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.63+50G>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.63+50G>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.63+50G>C
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.63+50G>C
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5414
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4675
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5506
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4711
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-53459241-GGAAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459241
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459237
    reference: chr 19
allele count: 19
allele frequency: 1.583755668178181e-4
allele num: 119968
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.63+35_63+38delTTTC
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.63+35_63+38delTTTC
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.63+35_63+38delTTTC
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.63+35_63+38delTTTC
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.63+35_63+38delTTTC
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.63+35_63+38delTTTC
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.63+35_63+38delTTTC
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.63+35_63+38delTTTC
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.63+35_63+38delTTTC
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.63+35_63+38delTTTC
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5194
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5510
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4711
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5414
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: GGAAA
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

19-53459243-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459243
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459243
    reference: chr 19
allele count: 2
allele frequency: 1.667444807576869e-5
allele num: 119944
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.63+37T>A
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.63+37T>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.63+37T>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.63+37T>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.63+37T>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.63+37T>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.63+37T>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.63+37T>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.63+37T>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.63+37T>A
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5250
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4709
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 7.75e1
  variant carriers: 0
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: A
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/19-53459245-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459245
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459245
    reference: chr 19
allele count: 1
allele frequency: 8.335695113615524e-6
allele num: 119966
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.63+35T>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.63+35T>G
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.63+35T>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.63+35T>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.63+35T>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.63+35T>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.63+35T>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.63+35T>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.63+35T>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.63+35T>G
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5508
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5250
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50520
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

19-53459252-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459252
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459252
    reference: chr 19
allele count: 1
allele frequency: 8.329585020074299e-6
allele num: 120054
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.63+28C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.63+28C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.63+28C>T
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.63+28C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.63+28C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.63+28C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.63+28C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.63+28C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.63+28C>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.63+28C>T
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5512
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4713
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50532
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

19-53459255-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459255
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459255
    reference: chr 19
allele count: 166
allele frequency: 1.381974391848016e-3
allele num: 120118
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.63+25C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.63+25C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.63+25C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.63+25C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.63+25C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.63+25C>A
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.63+25C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.63+25C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.63+25C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.63+25C>A
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5242
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4709
  bin: 7.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4670
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 7.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 5187
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5400
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5569
  bin: 9.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3807
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50541
  bin: 9.75e1
  variant carriers: 165
num of homozygotes: 1
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD

19-53459265-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459265
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459265
    reference: chr 19
allele count: 505
allele frequency: 4.19205418956386e-3
allele num: 120466
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.63+15T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.63+15T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.63+15T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.63+15T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.63+15T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.63+15T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.63+15T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.63+15T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.63+15T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.63+15T>C
  variant of: http://identifiers.org/hgnc/13827
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4675
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 7.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 8.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 9.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 3790
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5205
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5830
  bin: 9.75e1
  variant carriers: 360
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 8.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 6.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 2
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

19-53459269-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459269
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459269
    reference: chr 19
allele count: 3
allele frequency: 2.486407638244265e-5
allele num: 120656
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.63+11T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.63+11T>C
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.63+11T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.63+11T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.63+11T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.63+11T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.63+11T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.63+11T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.63+11T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.63+11T>C
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5373
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-53459281-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459281
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459281
    reference: chr 19
allele count: 1
allele frequency: 8.261595148791329e-6
allele num: 121042
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.62A>G
  hgvsp: ENSP00000472475.1:p.Gln21Arg
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.62A>G
  hgvsp: ENSP00000375656.3:p.Gln21Arg
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.62A>G
  hgvsp: ENSP00000350295.4:p.Gln21Arg
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.62A>G
  hgvsp: ENSP00000471215.1:p.Gln21Arg
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.62A>G
  hgvsp: ENSP00000408965.2:p.Gln21Arg
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.62A>G
  hgvsp: ENSP00000470838.1:p.Gln21Arg
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.62A>G
  hgvsp: ENSP00000438519.1:p.Gln21Arg
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.62A>G
  hgvsp: ENSP00000469688.1:p.Gln21Arg
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.62A>G
  hgvsp: ENSP00000333199.8:p.Gln21Arg
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.62A>G
  hgvsp: ENSP00000403266.2:p.Gln21Arg
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5165
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln21Arg
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

19-53459288-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459288
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459288
    reference: chr 19
allele count: 2
allele frequency: 1.651254953764861e-5
allele num: 121120
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.55C>G
  hgvsp: ENSP00000375656.3:p.Leu19Val
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.55C>G
  hgvsp: ENSP00000438519.1:p.Leu19Val
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.55C>G
  hgvsp: ENSP00000472475.1:p.Leu19Val
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.55C>G
  hgvsp: ENSP00000408965.2:p.Leu19Val
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.55C>G
  hgvsp: ENSP00000350295.4:p.Leu19Val
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.55C>G
  hgvsp: ENSP00000470838.1:p.Leu19Val
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.55C>G
  hgvsp: ENSP00000471215.1:p.Leu19Val
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.55C>G
  hgvsp: ENSP00000469688.1:p.Leu19Val
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.55C>G
  hgvsp: ENSP00000333199.8:p.Leu19Val
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.55C>G
  hgvsp: ENSP00000403266.2:p.Leu19Val
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu19Val
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-53459295-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459295
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459295
    reference: chr 19
allele count: 1
allele frequency: 8.252731654177533e-6
allele num: 121172
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.48G>T
  hgvsp: ENST00000357666.4:c.48G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.48G>T
  hgvsp: ENST00000444460.2:c.48G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.48G>T
  hgvsp: ENST00000457013.2:c.48G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.48G>T
  hgvsp: ENST00000438970.2:c.48G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.48G>T
  hgvsp: ENST00000332302.8:c.48G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.48G>T
  hgvsp: ENST00000434371.2:c.48G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.48G>T
  hgvsp: ENST00000391786.2:c.48G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.48G>T
  hgvsp: ENST00000391777.3:c.48G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.48G>T
  hgvsp: ENST00000535506.1:c.48G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.48G>T
  hgvsp: ENST00000270457.4:c.48G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.552G>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly16Gly
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

19-53459295-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459295
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459295
    reference: chr 19
allele count: 1
allele frequency: 8.252731654177533e-6
allele num: 121172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.48G>A
  hgvsp: ENST00000332302.8:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.48G>A
  hgvsp: ENST00000391786.2:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.48G>A
  hgvsp: ENST00000457013.2:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.48G>A
  hgvsp: ENST00000270457.4:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.48G>A
  hgvsp: ENST00000357666.4:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.48G>A
  hgvsp: ENST00000535506.1:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.48G>A
  hgvsp: ENST00000438970.2:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.48G>A
  hgvsp: ENST00000434371.2:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.48G>A
  hgvsp: ENST00000444460.2:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.552G>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.48G>A
  hgvsp: ENST00000391777.3:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13827
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly16Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

19-53459298-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459298
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459299
    reference: chr 19
allele count: 47
allele frequency: 3.877759809907264e-4
allele num: 121204
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.44dupC
  hgvsp: ENSP00000438519.1:p.Gly16ArgfsTer79
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.44dupC
  hgvsp: ENSP00000333199.8:p.Gly16ArgfsTer45
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.44dupC
  hgvsp: ENSP00000470838.1:p.Gly16ArgfsTer50
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.44dupC
  hgvsp: ENSP00000469688.1:p.Gly16ArgfsTer83
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.44dupC
  hgvsp: ENSP00000375656.3:p.Gly16ArgfsTer79
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.44dupC
  hgvsp: ENSP00000408965.2:p.Gly16ArgfsTer50
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.44dupC
  hgvsp: ENSP00000403266.2:p.Gly16ArgfsTer50
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.548dupC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.44dupC
  hgvsp: ENSP00000471215.1:p.Gly16ArgfsTer11
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.44dupC
  hgvsp: ENSP00000350295.4:p.Gly16ArgfsTer50
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.44dupC
  hgvsp: ENSP00000472475.1:p.Gly16ArgfsTer50
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4743
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5368
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5773
  bin: 9.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5201
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly16ArgfsTer79
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

19-53459300-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459300
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459300
    reference: chr 19
allele count: 1
allele frequency: 8.250280509537325e-6
allele num: 121208
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.43C>G
  hgvsp: ENSP00000438519.1:p.Pro15Ala
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.43C>G
  hgvsp: ENSP00000333199.8:p.Pro15Ala
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.43C>G
  hgvsp: ENSP00000403266.2:p.Pro15Ala
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.43C>G
  hgvsp: ENSP00000375656.3:p.Pro15Ala
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.43C>G
  hgvsp: ENSP00000470838.1:p.Pro15Ala
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.43C>G
  hgvsp: ENSP00000350295.4:p.Pro15Ala
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.43C>G
  hgvsp: ENSP00000408965.2:p.Pro15Ala
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.547C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.43C>G
  hgvsp: ENSP00000472475.1:p.Pro15Ala
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.43C>G
  hgvsp: ENSP00000471215.1:p.Pro15Ala
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.43C>G
  hgvsp: ENSP00000469688.1:p.Pro15Ala
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4647
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5749
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5205
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro15Ala
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

19-53459324-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459324
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459324
    reference: chr 19
allele count: 1
allele frequency: 8.250416646040625e-6
allele num: 121206
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.19A>G
  hgvsp: ENSP00000408965.2:p.Thr7Ala
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.19A>G
  hgvsp: ENSP00000350295.4:p.Thr7Ala
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.19A>G
  hgvsp: ENSP00000471215.1:p.Thr7Ala
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.19A>G
  hgvsp: ENSP00000469688.1:p.Thr7Ala
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.19A>G
  hgvsp: ENSP00000438519.1:p.Thr7Ala
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.523A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.19A>G
  hgvsp: ENSP00000470838.1:p.Thr7Ala
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.19A>G
  hgvsp: ENSP00000333199.8:p.Thr7Ala
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.19A>G
  hgvsp: ENSP00000375656.3:p.Thr7Ala
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.19A>G
  hgvsp: ENSP00000403266.2:p.Thr7Ala
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.19A>G
  hgvsp: ENSP00000472475.1:p.Thr7Ala
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5749
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr7Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP

19-53459326-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459326
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459326
    reference: chr 19
allele count: 4
allele frequency: 3.300438958381465e-5
allele num: 121196
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.17C>A
  hgvsp: ENSP00000470838.1:p.Ala6Asp
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.17C>A
  hgvsp: ENSP00000472475.1:p.Ala6Asp
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.17C>A
  hgvsp: ENSP00000469688.1:p.Ala6Asp
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.17C>A
  hgvsp: ENSP00000333199.8:p.Ala6Asp
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.17C>A
  hgvsp: ENSP00000403266.2:p.Ala6Asp
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.17C>A
  hgvsp: ENSP00000350295.4:p.Ala6Asp
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.17C>A
  hgvsp: ENSP00000375656.3:p.Ala6Asp
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.521C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.17C>A
  hgvsp: ENSP00000438519.1:p.Ala6Asp
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.17C>A
  hgvsp: ENSP00000408965.2:p.Ala6Asp
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.17C>A
  hgvsp: ENSP00000471215.1:p.Ala6Asp
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5752
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5165
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala6Asp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

19-53459330-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459330
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459330
    reference: chr 19
allele count: 3
allele frequency: 2.475574333245313e-5
allele num: 121184
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.13G>A
  hgvsp: ENSP00000333199.8:p.Glu5Lys
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.517G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.13G>A
  hgvsp: ENSP00000469688.1:p.Glu5Lys
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.13G>A
  hgvsp: ENSP00000350295.4:p.Glu5Lys
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.13G>A
  hgvsp: ENSP00000375656.3:p.Glu5Lys
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.13G>A
  hgvsp: ENSP00000408965.2:p.Glu5Lys
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.13G>A
  hgvsp: ENSP00000403266.2:p.Glu5Lys
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.13G>A
  hgvsp: ENSP00000472475.1:p.Glu5Lys
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.13G>A
  hgvsp: ENSP00000471215.1:p.Glu5Lys
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.13G>A
  hgvsp: ENSP00000470838.1:p.Glu5Lys
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.13G>A
  hgvsp: ENSP00000438519.1:p.Glu5Lys
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5753
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4647
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5369
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu5Lys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP

19-53459335-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459335
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459335
    reference: chr 19
allele count: 1
allele frequency: 8.252595441266279e-6
allele num: 121174
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.8G>A
  hgvsp: ENSP00000438519.1:p.Arg3His
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.8G>A
  hgvsp: ENSP00000403266.2:p.Arg3His
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.8G>A
  hgvsp: ENSP00000472475.1:p.Arg3His
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.8G>A
  hgvsp: ENSP00000469688.1:p.Arg3His
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.8G>A
  hgvsp: ENSP00000333199.8:p.Arg3His
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.512G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.8G>A
  hgvsp: ENSP00000375656.3:p.Arg3His
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.8G>A
  hgvsp: ENSP00000470838.1:p.Arg3His
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.8G>A
  hgvsp: ENSP00000471215.1:p.Arg3His
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.8G>A
  hgvsp: ENSP00000350295.4:p.Arg3His
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.8G>A
  hgvsp: ENSP00000408965.2:p.Arg3His
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4647
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5753
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg3His
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

19-53459336-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459336
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459336
    reference: chr 19
allele count: 12
allele frequency: 9.904095343424506e-5
allele num: 121162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.7C>T
  hgvsp: ENSP00000469688.1:p.Arg3Cys
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.7C>T
  hgvsp: ENSP00000471215.1:p.Arg3Cys
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.7C>T
  hgvsp: ENSP00000470838.1:p.Arg3Cys
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.511C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.7C>T
  hgvsp: ENSP00000403266.2:p.Arg3Cys
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.7C>T
  hgvsp: ENSP00000350295.4:p.Arg3Cys
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.7C>T
  hgvsp: ENSP00000438519.1:p.Arg3Cys
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.7C>T
  hgvsp: ENSP00000408965.2:p.Arg3Cys
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.7C>T
  hgvsp: ENSP00000333199.8:p.Arg3Cys
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.7C>T
  hgvsp: ENSP00000375656.3:p.Arg3Cys
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.7C>T
  hgvsp: ENSP00000472475.1:p.Arg3Cys
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5759
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4646
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg3Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

19-53459341-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459341
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459342
    reference: chr 19
allele count: 1
allele frequency: 8.255456856982466e-6
allele num: 121132
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.1dupA
  hgvsp: ENSP00000470838.1:p.Met1?
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.1dupA
  hgvsp: ENSP00000403266.2:p.Met1?
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.1dupA
  hgvsp: ENSP00000408965.2:p.Met1?
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.1dupA
  hgvsp: ENSP00000438519.1:p.Met1?
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.1dupA
  hgvsp: ENSP00000375656.3:p.Met1?
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.1dupA
  hgvsp: ENSP00000469688.1:p.Met1?
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.1dupA
  hgvsp: ENSP00000333199.8:p.Met1?
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.1dupA
  hgvsp: ENSP00000471215.1:p.Met1?
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.1dupA
  hgvsp: ENSP00000472475.1:p.Met1?
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.505dupA
annotation: Annotation
  canonical: true
  consequence: start_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.1dupA
  hgvsp: ENSP00000350295.4:p.Met1?
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5759
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

19-53459347-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459347
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459346
    reference: chr 19
allele count: 1
allele frequency: 8.260776182530111e-6
allele num: 121054
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.-6delA
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.-6delA
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.-6delA
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.499delA
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.-6delA
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.-6delA
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.-6delA
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.-6delA
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.-6delA
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.-6delA
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.-6delA
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5760
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: CT
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum

19-53459351-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459351
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459351
    reference: chr 19
allele count: 3
allele frequency: 2.479133955871415e-5
allele num: 121010
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.-9C>G
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.-9C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.-9C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.496C>G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.-9C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.-9C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.-9C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.-9C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.-9C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.-9C>G
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.-9C>G
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4646
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5761
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

19-53459356-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459356
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459356
    reference: chr 19
allele count: 23
allele frequency: 1.902493093122901e-4
allele num: 120894
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.-14A>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.-14A>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.-14A>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.-14A>T
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.-14A>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.-14A>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.-14A>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.491A>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.-14A>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.-14A>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.-14A>T
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3773
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5781
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2656
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.-14A>T
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-53459358-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459358
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459358
    reference: chr 19
allele count: 1
allele frequency: 8.274446853227862e-6
allele num: 120854
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.-15-1G>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.-15-1G>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.-15-1G>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.490-1G>T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.-15-1G>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.-15-1G>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.-15-1G>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.-15-1G>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.-15-1G>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.-15-1G>T
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.-15-1G>T
  variant of: http://identifiers.org/hgnc/13827
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3772
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4689
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5370
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 2.75e1
  variant carriers: 0
hgvs: c.-15-1G>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

19-53459373-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459373
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459373
    reference: chr 19
allele count: 137
allele frequency: 1.135930219060412e-3
allele num: 120606
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.-15-16C>A
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.-15-16C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.-15-16C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.-15-16C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.-15-16C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.-15-16C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.490-16C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.-15-16C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.-15-16C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.-15-16C>A
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.-15-16C>A
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3766
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5155
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4679
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5835
  bin: 9.75e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 5357
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP

19-53459387-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459387
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459387
    reference: chr 19
allele count: 1
allele frequency: 8.317530026283395e-6
allele num: 120228
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.-15-30T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.-15-30T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.-15-30T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.490-30T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.-15-30T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.-15-30T>C
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.-15-30T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.-15-30T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.-15-30T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.-15-30T>C
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.-15-30T>C
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5161
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1006
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

19-53459388-T-TAGGGAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459388
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459394
    reference: chr 19
allele count: 1
allele frequency: 8.321959988016378e-6
allele num: 120164
alternate allele: TAGGGAC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  hgvsc: ENST00000357666.4:c.-15-32_-15-31insGTCCCT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  hgvsc: ENST00000444460.2:c.-15-32_-15-31insGTCCCT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  hgvsc: ENST00000434371.2:c.-15-32_-15-31insGTCCCT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  hgvsc: ENST00000391786.2:c.-15-32_-15-31insGTCCCT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  hgvsc: ENST00000438970.2:c.-15-32_-15-31insGTCCCT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  hgvsc: ENST00000535506.1:c.-15-32_-15-31insGTCCCT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.490-32_490-31insGTCCCT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  hgvsc: ENST00000391777.3:c.-15-32_-15-31insGTCCCT
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  hgvsc: ENST00000457013.2:c.-15-32_-15-31insGTCCCT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  hgvsc: ENST00000270457.4:c.-15-32_-15-31insGTCCCT
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  hgvsc: ENST00000332302.8:c.-15-32_-15-31insGTCCCT
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1458
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

19-53459389-T-TGAGAAAAGACACGGGTGAGTGCGAGCAAACGTGTGATG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53459389
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53459427
    reference: chr 19
allele count: 1
allele frequency: 8.331666999933347e-6
allele num: 120024
alternate allele: TGAGAAAAGACACGGGTGAGTGCGAGCAAACGTGTGATG
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000470838
  ensembl transcript: ENST00000535506
  gene symbol: ZNF816
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000333199
  ensembl transcript: ENST00000332302
  gene symbol: ZNF816
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000403266
  ensembl transcript: ENST00000444460
  gene symbol: ZNF816
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000221874
  ensembl protein: ENSP00000375656
  ensembl transcript: ENST00000391777
  gene symbol: ZNF321P
  variant of: http://identifiers.org/hgnc/13827
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000469688
  ensembl transcript: ENST00000438970
  gene symbol: ZNF816
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000471215
  ensembl transcript: ENST00000391786
  gene symbol: ZNF816
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000408965
  ensembl transcript: ENST00000457013
  gene symbol: ZNF816
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000438519
  ensembl transcript: ENST00000434371
  gene symbol: ZNF816
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000472475
  ensembl transcript: ENST00000270457
  gene symbol: ZNF816
  variant of: http://identifiers.org/hgnc/26995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000180257
  ensembl protein: ENSP00000350295
  ensembl transcript: ENST00000357666
  gene symbol: ZNF816
  variant of: http://identifiers.org/hgnc/26995
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

19-53473009-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53473009
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53473009
    reference: chr 19
allele count: 2
allele frequency: 1.649538953862396e-5
allele num: 121246
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000434269
  gene symbol: ZNF702P
  hgvsc: ENST00000434269.1:n.1120A>G
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000270443
  gene symbol: ZNF702P
  hgvsc: ENST00000270443.4:n.1485A>G
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.489+868A>G
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6939
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7692
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5399
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6357
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1556
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2551
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2976
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2005
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44133
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1950
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2306
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2317
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP

19-53473022-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53473022
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53473022
    reference: chr 19
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000434269
  gene symbol: ZNF702P
  hgvsc: ENST00000434269.1:n.1107A>C
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.489+855A>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000270443
  gene symbol: ZNF702P
  hgvsc: ENST00000270443.4:n.1472A>C
  variant of: http://identifiers.org/hgnc/25775
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5366
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5399
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6357
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6936
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2638
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1952
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2554
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2308
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2986
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1559
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2023
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44138
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

19-53473029-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53473029
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53473029
    reference: chr 19
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000434269
  gene symbol: ZNF702P
  hgvsc: ENST00000434269.1:n.1100C>G
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000270443
  gene symbol: ZNF702P
  hgvsc: ENST00000270443.4:n.1465C>G
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.489+848C>G
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3198
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7219
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5399
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6937
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2561
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2032
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1956
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1571
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2699
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44139
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2987
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2311
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP

19-53473030-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53473030
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53473030
    reference: chr 19
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.489+847A>G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000270443
  gene symbol: ZNF702P
  hgvsc: ENST00000270443.4:n.1464A>G
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000434269
  gene symbol: ZNF702P
  hgvsc: ENST00000434269.1:n.1099A>G
  variant of: http://identifiers.org/hgnc/25775
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5399
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7700
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3198
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2033
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1955
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44140
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2988
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2308
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2563
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2705
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ

19-53473034-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53473034
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53473034
    reference: chr 19
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000434269
  gene symbol: ZNF702P
  hgvsc: ENST00000434269.1:n.1095T>C
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.489+843T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000270443
  gene symbol: ZNF702P
  hgvsc: ENST00000270443.4:n.1460T>C
  variant of: http://identifiers.org/hgnc/25775
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6926
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5399
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2539
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1547
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2278
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2674
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1985
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1944
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44062
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2963
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

19-53473037-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53473037
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53473037
    reference: chr 19
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000270443
  gene symbol: ZNF702P
  hgvsc: ENST00000270443.4:n.1457A>G
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000434269
  gene symbol: ZNF702P
  hgvsc: ENST00000434269.1:n.1092A>G
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.489+840A>G
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5398
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1974
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2567
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2718
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44165
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1588
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2984
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2324
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2024
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

19-53473046-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53473046
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53473046
    reference: chr 19
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000434269
  gene symbol: ZNF702P
  hgvsc: ENST00000434269.1:n.1083A>T
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000270443
  gene symbol: ZNF702P
  hgvsc: ENST00000270443.4:n.1448A>T
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.489+831A>T
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5398
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6943
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2647
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2587
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1587
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44178
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2324
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2987
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2015
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ

19-53473067-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53473067
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53473067
    reference: chr 19
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.489+810G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000434269
  gene symbol: ZNF702P
  hgvsc: ENST00000434269.1:n.1062G>A
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000270443
  gene symbol: ZNF702P
  hgvsc: ENST00000270443.4:n.1427G>A
  variant of: http://identifiers.org/hgnc/25775
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5398
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3146
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6946
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3001
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44191
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2336
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1591
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2493
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2606
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2019
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1991
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

19-53473075-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53473075
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53473075
    reference: chr 19
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000270443
  gene symbol: ZNF702P
  hgvsc: ENST00000270443.4:n.1419C>A
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000434269
  gene symbol: ZNF702P
  hgvsc: ENST00000434269.1:n.1054C>A
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.489+802C>A
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5488
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6930
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5398
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7738
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44198
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1579
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2348
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2459
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2000
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2622
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3007
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD

19-53473085-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53473085
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53473085
    reference: chr 19
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.489+792G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000270443
  gene symbol: ZNF702P
  hgvsc: ENST00000270443.4:n.1409G>A
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000434269
  gene symbol: ZNF702P
  hgvsc: ENST00000434269.1:n.1044G>A
  variant of: http://identifiers.org/hgnc/25775
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6936
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5398
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2637
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44201
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2002
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2452
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1588
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2000
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2351
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3013
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/19-53473085-CAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53473085
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53473083
    reference: chr 19
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000434269
  gene symbol: ZNF702P
  hgvsc: ENST00000434269.1:n.1042_1043delTT
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.489+790_489+791delTT
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000270443
  gene symbol: ZNF702P
  hgvsc: ENST00000270443.4:n.1407_1408delTT
  variant of: http://identifiers.org/hgnc/25775
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5398
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6936
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3013
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2000
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2002
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2452
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2351
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1588
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2637
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44201
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: CAA
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

19-53473086-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53473086
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53473086
    reference: chr 19
allele count: 119
allele frequency: 9.81491867638811e-4
allele num: 121244
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.489+791T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000434269
  gene symbol: ZNF702P
  hgvsc: ENST00000434269.1:n.1043T>C
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000270443
  gene symbol: ZNF702P
  hgvsc: ENST00000270443.4:n.1408T>C
  variant of: http://identifiers.org/hgnc/25775
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7236
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4803
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 5402
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7731
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6365
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 6.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2629
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1995
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1995
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2455
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1588
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3005
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2350
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44245
  bin: 9.75e1
  variant carriers: 117
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

19-53473090-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53473090
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53473090
    reference: chr 19
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000270443
  gene symbol: ZNF702P
  hgvsc: ENST00000270443.4:n.1404C>T
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000434269
  gene symbol: ZNF702P
  hgvsc: ENST00000434269.1:n.1039C>T
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.489+787C>T
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7739
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6924
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5402
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1998
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2634
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2470
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2003
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44230
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3007
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1584
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2361
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-53473091-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53473091
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53473091
    reference: chr 19
allele count: 2
allele frequency: 1.649430121892886e-5
allele num: 121254
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269082
  ensembl transcript: ENST00000600068
  gene symbol: CTD-2620I22.1
  hgvsc: ENST00000600068.1:n.489+786A>G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000270443
  gene symbol: ZNF702P
  hgvsc: ENST00000270443.4:n.1403A>G
  variant of: http://identifiers.org/hgnc/25775
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000242779
  ensembl transcript: ENST00000434269
  gene symbol: ZNF702P
  hgvsc: ENST00000434269.1:n.1038A>G
  variant of: http://identifiers.org/hgnc/25775
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6924
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5402
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7739
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1998
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44228
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2003
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2454
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 2332
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3275
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26544
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 226
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3522
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3996
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2170
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9530
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.671522719389525e-5
allele num: 11532
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10034
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65924
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14980
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

DP
type: SiteQuality
SIO_000300: 2.222236e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.434e0

QD
type: SiteQuality
SIO_000300: 1.534e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.99e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.87e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 26547
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2329
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10020
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14840
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51804960986125e-5
allele num: 65874
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.203e0

MQRankSum
type: SiteQuality
SIO_000300: -4.72e-1

QD
type: SiteQuality
SIO_000300: 1.492e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 2.220216e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.101e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.1e-1

MQ
type: SiteQuality
SIO_000300: 5.935e1

GenotypeQuality
all individuals: 250
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8519
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.162520344106022e-4
allele num: 8602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14692
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9984
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.471017007983339e-4
allele num: 11524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.5194797301404e-4
allele num: 65812
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.75e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

QD
type: SiteQuality
SIO_000300: 1.577e1

DP
type: SiteQuality
SIO_000300: 2.220315e6

VQSLOD
type: SiteQuality
SIO_000300: 5.87e0

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 122

GenotypeQuality
all individuals: 2771
bin: 2.5e0
variant carriers: 100

GenotypeQuality
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variant carriers: 162

GenotypeQuality
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variant carriers: 78

GenotypeQuality
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variant carriers: 114

GenotypeQuality
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variant carriers: 98

GenotypeQuality
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variant carriers: 55

GenotypeQuality
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variant carriers: 200

GenotypeQuality
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bin: 4.25e1
variant carriers: 94

GenotypeQuality
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bin: 9.25e1
variant carriers: 48

GenotypeQuality
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variant carriers: 235

GenotypeQuality
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GenotypeQuality
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variant carriers: 70

GenotypeQuality
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variant carriers: 145

GenotypeQuality
all individuals: 152
bin: 3.25e1
variant carriers: 106

GenotypeQuality
all individuals: 284
bin: 9.75e1
variant carriers: 284

East Asian
type: Population
allele count: 31
allele frequency: 4.305555555555556e-1
allele num: 72
num of homozygotes: 0

Other
type: Population
allele count: 9
allele frequency: 3.214285714285715e-1
allele num: 28
num of homozygotes: 0

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

Latino
type: Population
allele count: 12
allele frequency: 5.0e-1
allele num: 24
num of homozygotes: 0

African
type: Population
allele count: 31
allele frequency: 5.961538461538461e-1
allele num: 52
num of homozygotes: 5

South Asian
type: Population
allele count: 608
allele frequency: 4.75e-1
allele num: 1280
num of homozygotes: 50

European (Non-Finnish)
type: Population
allele count: 252
allele frequency: 4.666666666666667e-1
allele num: 540
num of homozygotes: 22

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

QD
type: SiteQuality
SIO_000300: 1.291e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

DP
type: SiteQuality
SIO_000300: 5.1853e4

VQSLOD
type: SiteQuality
SIO_000300: 4.96e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.178e-1

MQ
type: SiteQuality
SIO_000300: 5.766e1

GenotypeQuality
all individuals: 2771
bin: 2.5e0
variant carriers: 11

GenotypeQuality
all individuals: 126
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variant carriers: 11

GenotypeQuality
all individuals: 51
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1305
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 81
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variant carriers: 12

GenotypeQuality
all individuals: 98
bin: 4.25e1
variant carriers: 7

East Asian
type: Population
allele count: 1
allele frequency: 1.388888888888889e-2
allele num: 72
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.592592592592593e-2
allele num: 540
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 7.142857142857142e-2
allele num: 28
num of homozygotes: 0

South Asian
type: Population
allele count: 32
allele frequency: 2.5e-2
allele num: 1280
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 5.76923076923077e-2
allele num: 52
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.96e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 5.1853e4

QD
type: SiteQuality
SIO_000300: 1.291e1

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQ
type: SiteQuality
SIO_000300: 5.766e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.178e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 73
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variant carriers: 2

GenotypeQuality
all individuals: 346
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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
all individuals: 284
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.851851851851852e-3
allele num: 540
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 3.571428571428571e-2
allele num: 28
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 4.6875e-3
allele num: 1280
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.96e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

MQ
type: SiteQuality
SIO_000300: 5.766e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

DP
type: SiteQuality
SIO_000300: 5.1853e4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.291e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.178e-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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GenotypeQuality
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GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2622
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 88
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1050
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 100
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.479e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.04e-2

MQ
type: SiteQuality
SIO_000300: 5.425e1

VQSLOD
type: SiteQuality
SIO_000300: 5.8e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.6723e4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2132
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 3.348961821835231e-4
allele num: 5972
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 102
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.03653e5

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.57e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.278e0

MQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 83
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variant carriers: 0

GenotypeQuality
all individuals: 47
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 738
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4010
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.455604075691412e-4
allele num: 6870
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 110
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 88
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2456
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-1

QD
type: SiteQuality
SIO_000300: 1.037e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.801e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.01e-2

DP
type: SiteQuality
SIO_000300: 1.159e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.94e-1

MQ
type: SiteQuality
SIO_000300: 5.741e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.701e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.457e0

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

GenotypeQuality
all individuals: 32
bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Latino
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South Asian
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European (Finnish)
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QD
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DP
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ReadPosRankSum
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MQ
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FS
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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European (Finnish)
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European (Non-Finnish)
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African
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Other
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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VQSLOD
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QD
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DP
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BaseQRankSum
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MQ
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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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Latino
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South Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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East Asian
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MQ
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ClippingRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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FS
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QD
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MQRankSum
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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South Asian
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European (Non-Finnish)
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Latino
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Other
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ReadPosRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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QD
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MQRankSum
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VQSLOD
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FS
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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Latino
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South Asian
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African
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East Asian
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FS
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQ
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DP
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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African
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Other
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European (Finnish)
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ReadPosRankSum
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FS
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DP
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MQ
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BaseQRankSum
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MQRankSum
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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African
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Latino
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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DP
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QD
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FS
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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East Asian
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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DP
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FS
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 1

African
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allele frequency: 0.0e0
allele num: 26
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 332
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1012
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

FS
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DP
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QD
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BaseQRankSum
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SIO_000300: -3.87e-1

ReadPosRankSum
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SIO_000300: -1.18e-1

InbreedingCoeff
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SIO_000300: 5.072e-1

VQSLOD
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ClippingRankSum
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SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 5.855e1

GenotypeQuality
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variant carriers: 6

GenotypeQuality
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variant carriers: 19

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

South Asian
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allele count: 82
allele frequency: 8.102766798418973e-2
allele num: 1012
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 6.927710843373494e-2
allele num: 332
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 26
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East Asian
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allele count: 5
allele frequency: 1.0e-1
allele num: 50
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: -3.87e-1

MQRankSum
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FS
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ClippingRankSum
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MQ
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DP
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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QD
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SIO_000300: 1.585e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.444444444444444e-3
allele num: 450
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African
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allele frequency: 1.5e-1
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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FS
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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MQ
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ReadPosRankSum
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QD
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VQSLOD
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 70
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 3
allele frequency: 2.645502645502645e-3
allele num: 1134
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 450
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
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MQRankSum
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SIO_000300: -4.21e-1

ReadPosRankSum
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DP
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 1.882e-1

BaseQRankSum
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SIO_000300: -7.36e-1

VQSLOD
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SIO_000300: 1.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

African
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allele count: 1
allele frequency: 2.5e-2
allele num: 40
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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 16
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Other
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1134
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 450
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

DP
type: SiteQuality
SIO_000300: 5.0463e4

MQ
type: SiteQuality
SIO_000300: 5.843e1

QD
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ClippingRankSum
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SIO_000300: 7.36e-1

VQSLOD
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ReadPosRankSum
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SIO_000300: 3.58e-1

InbreedingCoeff
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SIO_000300: 1.882e-1

MQRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2286
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European (Finnish)
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allele frequency: NaN
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.506265664160401e-3
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Latino
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African
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allele frequency: 8.823529411764706e-2
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FS
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MQ
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ReadPosRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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QD
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BaseQRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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East Asian
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South Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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DP
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MQ
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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FS
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
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East Asian
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allele frequency: 3.448275862068965e-2
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Latino
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South Asian
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African
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
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DP
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MQRankSum
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FS
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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African
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Latino
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East Asian
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Other
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ClippingRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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MQ
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BaseQRankSum
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FS
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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European (Finnish)
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Latino
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East Asian
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South Asian
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InbreedingCoeff
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ReadPosRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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FS
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DP
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Non-Finnish)
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Latino
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European (Finnish)
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South Asian
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MQ
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MQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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ClippingRankSum
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DP
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BaseQRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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South Asian
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African
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East Asian
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European (Finnish)
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Other
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MQ
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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VQSLOD
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QD
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FS
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele num: 6614
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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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European (Non-Finnish)
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allele frequency: 1.962619644312932e-4
allele num: 66238
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InbreedingCoeff
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FS
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BaseQRankSum
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MQRankSum
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DP
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ClippingRankSum
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QD
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VQSLOD
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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East Asian
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South Asian
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Other
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European (Finnish)
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BaseQRankSum
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FS
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InbreedingCoeff
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MQ
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MQRankSum
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QD
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ClippingRankSum
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ReadPosRankSum
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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European (Non-Finnish)
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Other
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East Asian
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African
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South Asian
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ReadPosRankSum
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MQ
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BaseQRankSum
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FS
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MQRankSum
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ClippingRankSum
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QD
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VQSLOD
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DP
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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Latino
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South Asian
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East Asian
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Other
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DP
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MQ
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 11564
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Other
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European (Finnish)
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African
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European (Non-Finnish)
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allele num: 66270
num of homozygotes: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15736
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.903e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 6.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.87e-1

DP
type: SiteQuality
SIO_000300: 3.771444e6

QD
type: SiteQuality
SIO_000300: 1.529e1

GenotypeQuality
all individuals: 346
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50576
bin: 9.75e1
variant carriers: 501

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

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 579
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5174
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 389
allele frequency: 5.861788372863989e-3
allele num: 66362
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 61
allele frequency: 9.222860598729966e-3
allele num: 6614
num of homozygotes: 0

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

Other
type: Population
allele count: 4
allele frequency: 4.474272930648769e-3
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 5.770340450086555e-4
allele num: 10398
num of homozygotes: 0

Latino
type: Population
allele count: 19
allele frequency: 1.641894227445558e-3
allele num: 11572
num of homozygotes: 0

South Asian
type: Population
allele count: 26
allele frequency: 1.627644922999875e-3
allele num: 15974
num of homozygotes: 1

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: 3.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.21e-1

FS
type: SiteQuality
SIO_000300: 2.899e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.26e0

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

DP
type: SiteQuality
SIO_000300: 3.804734e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.05e-1

QD
type: SiteQuality
SIO_000300: 1.608e1

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50546
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 715
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5531
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 135
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.214267959234402e-5
allele num: 16092
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.010687942194791e-5
allele num: 66430
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.286e0

QD
type: SiteQuality
SIO_000300: 1.175e1

DP
type: SiteQuality
SIO_000300: 3.800689e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.02e0

FS
type: SiteQuality
SIO_000300: 1.7153e1

MQRankSum
type: SiteQuality
SIO_000300: -5.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.44e-1

GenotypeDepth
all individuals: 5208
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50547
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6112
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 577
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 929
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66534
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16354
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.36e-1

FS
type: SiteQuality
SIO_000300: 7.461e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 3.808063e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.277e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-2

GenotypeQuality
all individuals: 361
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6236
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 181
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 942
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 575
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50546
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 392
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502584445245823e-5
allele num: 66552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.49e-1

QD
type: SiteQuality
SIO_000300: 1.347e1

MQ
type: SiteQuality
SIO_000300: 5.952e1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 4.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.66e-1

DP
type: SiteQuality
SIO_000300: 3.809755e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.686e0

GenotypeDepth
all individuals: 2015
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50546
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6281
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 392
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 360
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 716
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 576
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 945
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66564
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.810691e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.984e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.043e0

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.09e-1

FS
type: SiteQuality
SIO_000300: 5.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

QD
type: SiteQuality
SIO_000300: 1.315e1

GenotypeDepth
all individuals: 3309
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6281
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50546
bin: 9.75e1
variant carriers: 1

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

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

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

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

GenotypeQuality
all individuals: 576
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 945
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 146
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502313562886846e-5
allele num: 66564
num of homozygotes: 0

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

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.315e1

MQ
type: SiteQuality
SIO_000300: 5.984e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.043e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

FS
type: SiteQuality
SIO_000300: 5.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 3.810691e6

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.34e-1

GenotypeDepth
all individuals: 3776
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6301
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50555
bin: 9.75e1
variant carriers: 47

GenotypeQuality
all individuals: 943
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 8.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 3
allele frequency: 3.303964757709251e-3
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 40
allele frequency: 3.454828122300916e-3
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.00817111271329e-5
allele num: 66576
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.351e1

DP
type: SiteQuality
SIO_000300: 3.813772e6

MQ
type: SiteQuality
SIO_000300: 6.015e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-2

GenotypeDepth
all individuals: 5369
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 939
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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East Asian
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allele num: 8654
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African
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Latino
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BaseQRankSum
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SIO_000300: -3.06e-1

MQ
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MQRankSum
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InbreedingCoeff
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FS
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DP
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ClippingRankSum
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QD
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VQSLOD
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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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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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European (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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QD
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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MQ
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FS
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InbreedingCoeff
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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

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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African
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allele num: 10398
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Latino
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Other
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European (Finnish)
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East Asian
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InbreedingCoeff
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ReadPosRankSum
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QD
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MQRankSum
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FS
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQ
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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

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

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

Other
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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South Asian
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.506805275966709e-5
allele num: 66566
num of homozygotes: 0

VQSLOD
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FS
type: SiteQuality
SIO_000300: 5.25e-1

InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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MQ
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QD
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DP
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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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bin: 9.25e1
variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66564
num of homozygotes: 0

East Asian
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MQ
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SIO_000300: 5.809e1

ClippingRankSum
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BaseQRankSum
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DP
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FS
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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QD
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MQRankSum
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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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East Asian
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allele frequency: 1.271088513981974e-3
allele num: 8654
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African
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num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

European (Non-Finnish)
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East Asian
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African
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Other
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Latino
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European (Finnish)
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BaseQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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FS
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QD
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DP
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MQRankSum
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66522
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.809447e6

ClippingRankSum
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SIO_000300: 4.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.411e1

MQ
type: SiteQuality
SIO_000300: 6.029e1

VQSLOD
type: SiteQuality
SIO_000300: 2.19e0

MQRankSum
type: SiteQuality
SIO_000300: 2.38e0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66512
num of homozygotes: 0

African
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allele count: 3
allele frequency: 2.894635275955229e-4
allele num: 10364
num of homozygotes: 0

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

FS
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SIO_000300: 0.0e0

ReadPosRankSum
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VQSLOD
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QD
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BaseQRankSum
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DP
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InbreedingCoeff
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SIO_000300: -2.0e-4

MQ
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SIO_000300: 5.959e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.92e-1

MQRankSum
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SIO_000300: 2.76e-1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

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

Latino
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allele count: 21
allele frequency: 1.814098134070491e-3
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.008242584682029e-5
allele num: 66484
num of homozygotes: 0

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

East Asian
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allele count: 0
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

DP
type: SiteQuality
SIO_000300: 3.805178e6

ClippingRankSum
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SIO_000300: 3.5e-2

FS
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VQSLOD
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BaseQRankSum
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MQ
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SIO_000300: 5.959e1

MQRankSum
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SIO_000300: 1.73e-1

QD
type: SiteQuality
SIO_000300: 1.11e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

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

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

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

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

South Asian
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allele count: 1
allele frequency: 6.13195977434388e-5
allele num: 16308
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66470
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.144e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.03e-1

FS
type: SiteQuality
SIO_000300: 5.485e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.953e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 3.803144e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 137

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506024096385542e-5
allele num: 66400
num of homozygotes: 0

East Asian
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allele count: 0
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

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

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

African
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allele count: 135
allele frequency: 1.311443559354964e-2
allele num: 10294
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.144e1

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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FS
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 6.4e-3

MQ
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SIO_000300: 5.96e1

ClippingRankSum
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SIO_000300: 1.55e-1

DP
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SIO_000300: 3.790998e6

GenotypeQuality
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variant carriers: 1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66276
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: 0.0e0

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

Latino
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allele frequency: 8.640055296353897e-5
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European (Non-Finnish)
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South Asian
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African
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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FS
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MQ
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VQSLOD
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QD
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ClippingRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 10228
num of homozygotes: 0

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

Other
type: Population
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allele num: 888
num of homozygotes: 0

Latino
type: Population
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allele frequency: 8.641548565502938e-5
allele num: 11572
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East Asian
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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 count: 0
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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FS
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MQRankSum
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ReadPosRankSum
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DP
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BaseQRankSum
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ClippingRankSum
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MQ
type: SiteQuality
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QD
type: SiteQuality
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European (Non-Finnish)
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allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

South Asian
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allele num: 16504
num of homozygotes: 0

European (Finnish)
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Other
type: Population
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East Asian
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10318
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.359e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.581e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.78e-1

FS
type: SiteQuality
SIO_000300: 6.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

QD
type: SiteQuality
SIO_000300: 2.309e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.91e-1

DP
type: SiteQuality
SIO_000300: 3.460618e6

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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QD
type: SiteQuality
SIO_000300: 1.77e1

FS
type: SiteQuality
SIO_000300: 5.402e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.462283e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.95e0

MQ
type: SiteQuality
SIO_000300: 5.145e1

VQSLOD
type: SiteQuality
SIO_000300: -1.252e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.53e-1

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

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.568e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.632e0

FS
type: SiteQuality
SIO_000300: 2.695e0

QD
type: SiteQuality
SIO_000300: 1.308e1

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -8.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.5e-1

MQ
type: SiteQuality
SIO_000300: 4.936e1

DP
type: SiteQuality
SIO_000300: 3.463193e6

East Asian
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allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10322
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
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Other
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allele count: 0
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allele num: 906
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.03e-1

DP
type: SiteQuality
SIO_000300: 3.463323e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.05e0

FS
type: SiteQuality
SIO_000300: 2.889e0

VQSLOD
type: SiteQuality
SIO_000300: -1.54e0

QD
type: SiteQuality
SIO_000300: 1.203e1

MQ
type: SiteQuality
SIO_000300: 5.026e1

Other
type: Population
allele count: 0
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num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
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African
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allele count: 1
allele frequency: 9.682416731216112e-5
allele num: 10328
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66650
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
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Latino
type: Population
allele count: 0
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allele num: 11560
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MQ
type: SiteQuality
SIO_000300: 4.833e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.211e0

QD
type: SiteQuality
SIO_000300: 3.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e0

FS
type: SiteQuality
SIO_000300: 8.704000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -3.347e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

DP
type: SiteQuality
SIO_000300: 3.465179e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
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South Asian
type: Population
allele count: 0
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allele num: 16506
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
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MQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.315e1

DP
type: SiteQuality
SIO_000300: 3.464196e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.95e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 4.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.505e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.364e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10332
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South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66694
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 906
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.197e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.9e-2

DP
type: SiteQuality
SIO_000300: 3.464825e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

FS
type: SiteQuality
SIO_000300: 3.333e0

QD
type: SiteQuality
SIO_000300: 1.163e1

MQ
type: SiteQuality
SIO_000300: 4.88e1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
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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
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South Asian
type: Population
allele count: 0
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African
type: Population
allele count: 0
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Other
type: Population
allele count: 0
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MQ
type: SiteQuality
SIO_000300: 5.572e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.09e-1

FS
type: SiteQuality
SIO_000300: 1.052e1

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.311e1

MQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.473e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.518e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.04e-1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
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South Asian
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allele count: 0
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East Asian
type: Population
allele count: 0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
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MQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

FS
type: SiteQuality
SIO_000300: 1.412e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.668e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.9e-2

DP
type: SiteQuality
SIO_000300: 3.465174e6

MQ
type: SiteQuality
SIO_000300: 4.344e1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 8.82e0

Other
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allele count: 0
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allele num: 904
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
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African
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allele num: 10300
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East Asian
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allele count: 0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
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South Asian
type: Population
allele count: 0
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.387e1

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 4.559e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.96e-1

DP
type: SiteQuality
SIO_000300: 3.46558e6

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
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European (Finnish)
type: Population
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
allele num: 904
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
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Latino
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allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
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East Asian
type: Population
allele count: 0
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African
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DP
type: SiteQuality
SIO_000300: 3.46558e6

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.09e0

MQ
type: SiteQuality
SIO_000300: 4.559e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.71e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.387e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.96e-1

Other
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allele count: 0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
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East Asian
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allele count: 0
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African
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allele count: 116
allele frequency: 1.126432316954749e-2
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South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
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Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 3.999e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.09e-1

QD
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -3.212e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.98e-1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
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Other
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Latino
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allele count: 0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 0
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African
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South Asian
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allele frequency: 6.058403004967891e-5
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.695e0

VQSLOD
type: SiteQuality
SIO_000300: -2.165e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

QD
type: SiteQuality
SIO_000300: 8.66e0

MQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

MQ
type: SiteQuality
SIO_000300: 4.552e1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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