X-47836619-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836619
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836619
    reference: chr 0
allele count: 8
allele frequency: 9.332384540905008e-5
allele num: 85723
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.867C>G
  hgvsp: ENST00000305127.6:c.867C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.867C>G
  hgvsp: ENST00000396965.1:c.867C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25308G>C
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.810C>G
  hgvsp: ENST00000376943.3:c.810C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype depth: GenotypeDepth
  all individuals: 287
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  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2383
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro289Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

X-47836620-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836620
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836620
    reference: chr 0
allele count: 1
allele frequency: 1.166180758017493e-5
allele num: 85750
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.809C>T
  hgvsp: ENSP00000366142.3:p.Pro270Leu
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25307G>A
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.866C>T
  hgvsp: ENSP00000380165.1:p.Pro289Leu
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.866C>T
  hgvsp: ENSP00000306351.6:p.Pro289Leu
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro289Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

X-47836626-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836626
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836626
    reference: chr 0
allele count: 1
allele frequency: 1.164998776751284e-5
allele num: 85837
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.860A>C
  hgvsp: ENSP00000380165.1:p.Glu287Ala
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.803A>C
  hgvsp: ENSP00000366142.3:p.Glu268Ala
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.860A>C
  hgvsp: ENSP00000306351.6:p.Glu287Ala
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25301T>G
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 76
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  variant carriers: 0
hgvs: p.Glu287Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: T
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

X-47836631-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836631
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836631
    reference: chr 0
allele count: 25
allele frequency: 2.91046253070538e-4
allele num: 85897
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.855A>G
  hgvsp: ENST00000396965.1:c.855A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.798A>G
  hgvsp: ENST00000376943.3:c.798A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.855A>G
  hgvsp: ENST00000305127.6:c.855A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25296T>C
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 3
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1331
  bin: 9.75e1
  variant carriers: 17
hgvs: p.Thr285Thr
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

X-47836641-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836641
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836641
    reference: chr 0
allele count: 2
allele frequency: 2.325419156803014e-5
allele num: 86006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.788G>A
  hgvsp: ENSP00000366142.3:p.Arg263Gln
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.845G>A
  hgvsp: ENSP00000306351.6:p.Arg282Gln
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25286C>T
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.845G>A
  hgvsp: ENSP00000380165.1:p.Arg282Gln
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 45374
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1371
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6419
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 1314
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 470
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg282Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

X-47836650-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836650
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836650
    reference: chr 0
allele count: 1
allele frequency: 1.159245562987608e-5
allele num: 86263
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25277A>G
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.779T>C
  hgvsp: ENSP00000366142.3:p.Ile260Thr
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.836T>C
  hgvsp: ENSP00000380165.1:p.Ile279Thr
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.836T>C
  hgvsp: ENSP00000306351.6:p.Ile279Thr
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
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genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 7.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile279Thr
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

X-47836654-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836654
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836654
    reference: chr 0
allele count: 1
allele frequency: 1.158600873585059e-5
allele num: 86311
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.832A>G
  hgvsp: ENSP00000380165.1:p.Ile278Val
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.832A>G
  hgvsp: ENSP00000306351.6:p.Ile278Val
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.775A>G
  hgvsp: ENSP00000366142.3:p.Ile259Val
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25273T>C
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 398
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 191
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
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  variant carriers: 0
hgvs: p.Ile278Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: T
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS

X-47836690-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836690
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836690
    reference: chr 0
allele count: 2
allele frequency: 2.31000231000231e-5
allele num: 86580
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.796G>A
  hgvsp: ENSP00000306351.6:p.Glu266Lys
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25237C>T
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.796G>A
  hgvsp: ENSP00000380165.1:p.Glu266Lys
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.739G>A
  hgvsp: ENSP00000366142.3:p.Glu247Lys
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 22212
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 929
  bin: 1.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 556
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 293
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46513
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu266Lys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

X-47836691-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836691
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836691
    reference: chr 0
allele count: 21
allele frequency: 2.426202992317024e-4
allele num: 86555
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.738C>T
  hgvsp: ENST00000376943.3:c.738C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.795C>T
  hgvsp: ENST00000305127.6:c.795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.795C>T
  hgvsp: ENST00000396965.1:c.795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25236G>A
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5825
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22199
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1150
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46513
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1567
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 9.75e1
  variant carriers: 17
hgvs: p.Thr265Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

X-47836718-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836718
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836718
    reference: chr 0
allele count: 1
allele frequency: 1.158091002790999e-5
allele num: 86349
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.768T>C
  hgvsp: ENST00000396965.1:c.768T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.711T>C
  hgvsp: ENST00000376943.3:c.711T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.768T>C
  hgvsp: ENST00000305127.6:c.768T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25209A>G
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 21180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27696
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1278
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
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genotype quality: GenotypeQuality
  all individuals: 548
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1363
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45630
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
hgvs: p.His256His
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

X-47836742-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836742
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836742
    reference: chr 0
allele count: 1
allele frequency: 1.161615574941629e-5
allele num: 86087
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.687C>T
  hgvsp: ENST00000376943.3:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.744C>T
  hgvsp: ENST00000305127.6:c.744C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25185G>A
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.744C>T
  hgvsp: ENST00000396965.1:c.744C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6368
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1278
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 548
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
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genotype quality: GenotypeQuality
  all individuals: 569
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1348
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 138
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44975
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2272
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
hgvs: p.His248His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

X-47836765-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836765
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836765
    reference: chr 0
allele count: 1
allele frequency: 1.163358849670769e-5
allele num: 85958
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.721A>G
  hgvsp: ENSP00000306351.6:p.Lys241Glu
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.721A>G
  hgvsp: ENSP00000380165.1:p.Lys241Glu
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25162T>C
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.664A>G
  hgvsp: ENSP00000366142.3:p.Lys222Glu
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5762
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20565
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44771
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6369
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1344
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genotype quality: GenotypeQuality
  all individuals: 2255
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Lys241Glu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

X-47836766-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836766
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836766
    reference: chr 0
allele count: 1
allele frequency: 1.163886916747169e-5
allele num: 85919
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.720G>C
  hgvsp: ENSP00000380165.1:p.Arg240Ser
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.720G>C
  hgvsp: ENSP00000306351.6:p.Arg240Ser
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25161C>G
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.663G>C
  hgvsp: ENSP00000366142.3:p.Arg221Ser
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.75e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
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genotype depth: GenotypeDepth
  all individuals: 27414
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1341
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6357
  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1276
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 44760
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg240Ser
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-47836782-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836782
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836782
    reference: chr 0
allele count: 142
allele frequency: 1.653392948628382e-3
allele num: 85884
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.647A>C
  hgvsp: ENSP00000366142.3:p.Glu216Ala
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.704A>C
  hgvsp: ENSP00000306351.6:p.Glu235Ala
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.704A>C
  hgvsp: ENSP00000380165.1:p.Glu235Ala
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25145T>G
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20537
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genotype depth: GenotypeDepth
  all individuals: 198
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 86
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 167
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 44675
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genotype quality: GenotypeQuality
  all individuals: 183
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 193
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 211
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  variant carriers: 0
hgvs: p.Glu235Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

X-47836794-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836794
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836794
    reference: chr 0
allele count: 3
allele frequency: 3.490604456338356e-5
allele num: 85945
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.635A>G
  hgvsp: ENSP00000366142.3:p.Glu212Gly
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.692A>G
  hgvsp: ENSP00000380165.1:p.Glu231Gly
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.692A>G
  hgvsp: ENSP00000306351.6:p.Glu231Gly
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25133T>C
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1152
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu231Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

X-47836796-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836796
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836795
    reference: chr 0
allele count: 1
allele frequency: 1.163710841130196e-5
allele num: 85932
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.689delG
  hgvsp: ENSP00000380165.1:p.Gly230GlufsTer132
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25129delC
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.632delG
  hgvsp: ENSP00000366142.3:p.Gly211GlufsTer132
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.689delG
  hgvsp: ENSP00000306351.6:p.Gly230GlufsTer132
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 5744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 4.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly230GlufsTer132
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: TC
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum

X-47836809-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836809
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836809
    reference: chr 0
allele count: 1
allele frequency: 1.162007018522392e-5
allele num: 86058
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25118C>A
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.620G>T
  hgvsp: ENSP00000366142.3:p.Arg207Ile
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.677G>T
  hgvsp: ENSP00000306351.6:p.Arg226Ile
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.677G>T
  hgvsp: ENSP00000380165.1:p.Arg226Ile
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 191
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
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genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 107
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genotype quality: GenotypeQuality
  all individuals: 6356
  bin: 6.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 1343
  bin: 7.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1158
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg226Ile
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum

X-47836817-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836817
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836817
    reference: chr 0
allele count: 2
allele frequency: 2.318706161961625e-5
allele num: 86255
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25110T>C
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.612A>G
  hgvsp: ENST00000376943.3:c.612A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.669A>G
  hgvsp: ENST00000396965.1:c.669A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.669A>G
  hgvsp: ENST00000305127.6:c.669A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21677
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1166
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 425
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  variant carriers: 0
hgvs: p.Leu223Leu
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

X-47836835-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836835
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836835
    reference: chr 0
allele count: 1
allele frequency: 1.153748528970626e-5
allele num: 86674
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.651A>G
  hgvsp: ENST00000305127.6:c.651A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25092T>C
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.594A>G
  hgvsp: ENST00000376943.3:c.594A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.651A>G
  hgvsp: ENST00000396965.1:c.651A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 553
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  variant carriers: 0
hgvs: p.Arg217Arg
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

X-47836836-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836836
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836836
    reference: chr 0
allele count: 2
allele frequency: 2.307497057941251e-5
allele num: 86674
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.650G>A
  hgvsp: ENSP00000306351.6:p.Arg217Gln
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.593G>A
  hgvsp: ENSP00000366142.3:p.Arg198Gln
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25091C>T
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.650G>A
  hgvsp: ENSP00000380165.1:p.Arg217Gln
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1166
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg217Gln
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

X-47836837-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836837
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836837
    reference: chr 0
allele count: 1
allele frequency: 1.152976986579348e-5
allele num: 86732
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25090G>A
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.592C>T
  hgvsp: ENSP00000366142.3:p.Arg198Ter
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.649C>T
  hgvsp: ENSP00000380165.1:p.Arg217Ter
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.649C>T
  hgvsp: ENSP00000306351.6:p.Arg217Ter
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6424
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1210
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47168
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1226
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg217Ter
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

X-47836841-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836841
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836841
    reference: chr 0
allele count: 1
allele frequency: 1.15115864117234e-5
allele num: 86869
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.588T>C
  hgvsp: ENST00000376943.3:c.588T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.645T>C
  hgvsp: ENST00000305127.6:c.645T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.645T>C
  hgvsp: ENST00000396965.1:c.645T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25086A>G
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27840
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 273
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 140
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 12
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genotype quality: GenotypeQuality
  all individuals: 47506
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1074
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
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genotype quality: GenotypeQuality
  all individuals: 111
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genotype quality: GenotypeQuality
  all individuals: 180
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1227
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu215Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff

X-47836856-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836856
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836856
    reference: chr 0
allele count: 29
allele frequency: 3.331801470588235e-4
allele num: 87040
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.573G>A
  hgvsp: ENST00000376943.3:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25071C>T
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.630G>A
  hgvsp: ENST00000305127.6:c.630G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.630G>A
  hgvsp: ENST00000396965.1:c.630G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5751
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27866
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 618
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
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genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
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  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 404
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 195
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genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 1234
  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 172
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1341
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu210Glu
num of homozygotes: 1
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

X-47836860-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836860
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836860
    reference: chr 0
allele count: 4
allele frequency: 4.593899301727306e-5
allele num: 87072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.626A>T
  hgvsp: ENSP00000306351.6:p.Lys209Ile
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.626A>T
  hgvsp: ENSP00000380165.1:p.Lys209Ile
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25067T>A
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.569A>T
  hgvsp: ENSP00000366142.3:p.Lys190Ile
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27885
  bin: 2.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 5741
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 557
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1344
  bin: 7.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1214
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 872
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genotype quality: GenotypeQuality
  all individuals: 219
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1165
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47687
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys209Ile
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

X-47836865-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836865
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836865
    reference: chr 0
allele count: 1
allele frequency: 1.148593547201452e-5
allele num: 87063
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.621C>T
  hgvsp: ENST00000305127.6:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25062G>A
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.621C>T
  hgvsp: ENST00000396965.1:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.564C>T
  hgvsp: ENST00000376943.3:c.564C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5731
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 1336
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6369
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1215
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly207Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

X-47836865-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836865
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836865
    reference: chr 0
allele count: 15
allele frequency: 1.722890320802178e-4
allele num: 87063
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.621C>A
  hgvsp: ENST00000396965.1:c.621C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.621C>A
  hgvsp: ENST00000305127.6:c.621C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25062G>T
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.564C>A
  hgvsp: ENST00000376943.3:c.564C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5731
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 27828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 908
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 47493
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1336
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly207Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS

X-47836866-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836866
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836866
    reference: chr 0
allele count: 1
allele frequency: 1.148659514346757e-5
allele num: 87058
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.563G>T
  hgvsp: ENSP00000366142.3:p.Gly188Val
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.620G>T
  hgvsp: ENSP00000306351.6:p.Gly207Val
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.620G>T
  hgvsp: ENSP00000380165.1:p.Gly207Val
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25061C>A
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5730
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27827
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
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genotype depth: GenotypeDepth
  all individuals: 50
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 80
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 924
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6359
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1202
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gly207Val
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

X-47836868-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836868
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836868
    reference: chr 0
allele count: 20
allele frequency: 2.297794117647059e-4
allele num: 87040
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.561T>C
  hgvsp: ENST00000376943.3:c.561T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.618T>C
  hgvsp: ENST00000396965.1:c.618T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.618T>C
  hgvsp: ENST00000305127.6:c.618T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25059A>G
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5702
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 80
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  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
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  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 533
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genotype depth: GenotypeDepth
  all individuals: 610
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genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23022
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 444
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genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 49
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
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genotype depth: GenotypeDepth
  all individuals: 30
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 198
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 29
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genotype quality: GenotypeQuality
  all individuals: 216
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1329
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Tyr206Tyr
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

X-47836873-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836873
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836873
    reference: chr 0
allele count: 1
allele frequency: 1.14888385933066e-5
allele num: 87041
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.613C>A
  hgvsp: ENSP00000306351.6:p.Pro205Thr
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25054G>T
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.556C>A
  hgvsp: ENSP00000366142.3:p.Pro186Thr
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.613C>A
  hgvsp: ENSP00000380165.1:p.Pro205Thr
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro205Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

X-47836908-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836908
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836908
    reference: chr 0
allele count: 1
allele frequency: 1.154761079932562e-5
allele num: 86598
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.521A>G
  hgvsp: ENSP00000366142.3:p.His174Arg
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.578A>G
  hgvsp: ENSP00000306351.6:p.His193Arg
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25019T>C
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.578A>G
  hgvsp: ENSP00000380165.1:p.His193Arg
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.His193Arg
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

X-47836922-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836922
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836922
    reference: chr 0
allele count: 3
allele frequency: 3.4716596847733e-5
allele num: 86414
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.507A>C
  hgvsp: ENST00000376943.3:c.507A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.564A>C
  hgvsp: ENST00000396965.1:c.564A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.564A>C
  hgvsp: ENST00000305127.6:c.564A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25005T>G
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 880
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hgvs: p.Ala188Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

X-47836926-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836926
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836926
    reference: chr 0
allele count: 1
allele frequency: 1.159339640140976e-5
allele num: 86256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.503G>A
  hgvsp: ENSP00000366142.3:p.Cys168Tyr
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.560G>A
  hgvsp: ENSP00000306351.6:p.Cys187Tyr
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-25001C>T
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.560G>A
  hgvsp: ENSP00000380165.1:p.Cys187Tyr
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1163
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  variant carriers: 0
hgvs: p.Cys187Tyr
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum

X-47836944-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836944
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836944
    reference: chr 0
allele count: 3
allele frequency: 3.485980548228541e-5
allele num: 86059
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.485A>G
  hgvsp: ENSP00000366142.3:p.Asn162Ser
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.542A>G
  hgvsp: ENSP00000306351.6:p.Asn181Ser
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.542A>G
  hgvsp: ENSP00000380165.1:p.Asn181Ser
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24983T>C
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: missense
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Asn181Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
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site quality: VQSLOD

X-47836956-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836956
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836956
    reference: chr 0
allele count: 2
allele frequency: 2.328153192480065e-5
allele num: 85905
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.530G>A
  hgvsp: ENSP00000306351.6:p.Ser177Asn
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.530G>A
  hgvsp: ENSP00000380165.1:p.Ser177Asn
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.473G>A
  hgvsp: ENSP00000366142.3:p.Ser158Asn
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24971C>T
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Ser177Asn
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

X-47836957-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836957
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836957
    reference: chr 0
allele count: 1
allele frequency: 1.163710841130196e-5
allele num: 85932
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.472A>C
  hgvsp: ENSP00000366142.3:p.Ser158Arg
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.529A>C
  hgvsp: ENSP00000306351.6:p.Ser177Arg
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24970T>G
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.529A>C
  hgvsp: ENSP00000380165.1:p.Ser177Arg
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Ser177Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

X-47836959-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836959
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836959
    reference: chr 0
allele count: 1
allele frequency: 1.16410369835745e-5
allele num: 85903
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24968C>G
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.470G>C
  hgvsp: ENSP00000366142.3:p.Arg157Thr
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.527G>C
  hgvsp: ENSP00000380165.1:p.Arg176Thr
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.527G>C
  hgvsp: ENSP00000306351.6:p.Arg176Thr
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Arg176Thr
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

X-47836975-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836975
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836975
    reference: chr 0
allele count: 2
allele frequency: 2.327638378101578e-5
allele num: 85924
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24952A>C
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.511T>G
  hgvsp: ENSP00000380165.1:p.Leu171Val
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.511T>G
  hgvsp: ENSP00000306351.6:p.Leu171Val
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.454T>G
  hgvsp: ENSP00000366142.3:p.Leu152Val
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Leu171Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
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site quality: DP
site quality: QD

X-47836984-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836984
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836984
    reference: chr 0
allele count: 1
allele frequency: 1.16342652379789e-5
allele num: 85953
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.502G>T
  hgvsp: ENSP00000306351.6:p.Val168Leu
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.445G>T
  hgvsp: ENSP00000366142.3:p.Val149Leu
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.502G>T
  hgvsp: ENSP00000380165.1:p.Val168Leu
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
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  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Val168Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

X-47836985-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836985
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836985
    reference: chr 0
allele count: 15
allele frequency: 1.745281921206339e-4
allele num: 85946
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.501G>A
  hgvsp: ENSP00000380165.1:p.Met167Ile
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.444G>A
  hgvsp: ENSP00000366142.3:p.Met148Ile
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24942C>T
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
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  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
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  hgvsc: ENST00000305127.6:c.501G>A
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  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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hgvs: p.Met167Ile
num of homozygotes: 1
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
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X-47836996-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047836996
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047836996
    reference: chr 0
allele count: 1
allele frequency: 1.161264849674265e-5
allele num: 86113
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.433G>A
  hgvsp: ENSP00000366142.3:p.Gly145Arg
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.490G>A
  hgvsp: ENSP00000380165.1:p.Gly164Arg
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24931C>T
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.490G>A
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  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1609
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genotype depth: GenotypeDepth
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hgvs: p.Gly164Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
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site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
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site quality: ClippingRankSum

X-47837002-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837002
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837002
    reference: chr 0
allele count: 1
allele frequency: 1.159259001646148e-5
allele num: 86262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24925A>T
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.484T>A
  hgvsp: ENSP00000306351.6:p.Ser162Thr
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
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  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
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  hgvsp: ENSP00000366142.3:p.Ser143Thr
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
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  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.484T>A
  hgvsp: ENSP00000380165.1:p.Ser162Thr
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 8.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 318
  bin: 4.75e1
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 5483
  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 560
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser162Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ

X-47837005-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837005
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837005
    reference: chr 0
allele count: 1
allele frequency: 1.159205248881367e-5
allele num: 86266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.481G>A
  hgvsp: ENSP00000306351.6:p.Glu161Lys
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.424G>A
  hgvsp: ENSP00000366142.3:p.Glu142Lys
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.481G>A
  hgvsp: ENSP00000380165.1:p.Glu161Lys
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24922C>T
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu161Lys
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

X-47837006-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837006
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837006
    reference: chr 0
allele count: 6
allele frequency: 6.948706961446257e-5
allele num: 86347
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24921G>A
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.480C>T
  hgvsp: ENST00000305127.6:c.480C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.423C>T
  hgvsp: ENST00000376943.3:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.480C>T
  hgvsp: ENST00000396965.1:c.480C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1146
  bin: 7.25e1
  variant carriers: 0
hgvs: p.His160His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

X-47837014-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837014
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837014
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 86470
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.415G>A
  hgvsp: ENSP00000366142.3:p.Asp139Asn
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.472G>A
  hgvsp: ENSP00000306351.6:p.Asp158Asn
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24913C>T
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.472G>A
  hgvsp: ENSP00000380165.1:p.Asp158Asn
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1171
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  variant carriers: 0
hgvs: p.Asp158Asn
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

X-47837015-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837015
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837015
    reference: chr 0
allele count: 13
allele frequency: 1.502247593514913e-4
allele num: 86537
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.471C>T
  hgvsp: ENST00000305127.6:c.471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.414C>T
  hgvsp: ENST00000376943.3:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24912G>A
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.471C>T
  hgvsp: ENST00000396965.1:c.471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 3
genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 1
hgvs: p.Pro157Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD

X-47837018-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837018
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837018
    reference: chr 0
allele count: 1
allele frequency: 1.154534433989494e-5
allele num: 86615
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.468A>G
  hgvsp: ENST00000396965.1:c.468A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.411A>G
  hgvsp: ENST00000376943.3:c.411A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.468A>G
  hgvsp: ENST00000305127.6:c.468A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24909T>C
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 1.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 361
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hgvs: p.Arg156Arg
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

X-47837035-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837035
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837035
    reference: chr 0
allele count: 2
allele frequency: 2.300939933963024e-5
allele num: 86921
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.394G>C
  hgvsp: ENSP00000366142.3:p.Val132Leu
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.451G>C
  hgvsp: ENSP00000306351.6:p.Val151Leu
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24892C>G
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.451G>C
  hgvsp: ENSP00000380165.1:p.Val151Leu
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Val151Leu
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

X-47837053-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837053
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837053
    reference: chr 0
allele count: 4
allele frequency: 4.598229681572594e-5
allele num: 86990
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24874G>A
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.433C>T
  hgvsp: ENSP00000306351.6:p.His145Tyr
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.376C>T
  hgvsp: ENSP00000366142.3:p.His126Tyr
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.433C>T
  hgvsp: ENSP00000380165.1:p.His145Tyr
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.His145Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

X-47837065-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837065
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837065
    reference: chr 0
allele count: 16
allele frequency: 1.840900200197897e-4
allele num: 86914
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.364G>A
  hgvsp: ENSP00000366142.3:p.Gly122Arg
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24862C>T
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.421G>A
  hgvsp: ENSP00000380165.1:p.Gly141Arg
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.421G>A
  hgvsp: ENSP00000306351.6:p.Gly141Arg
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 210
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 505
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly141Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

X-47837067-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837067
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837067
    reference: chr 0
allele count: 1
allele frequency: 1.151330938564981e-5
allele num: 86856
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.419T>C
  hgvsp: ENSP00000306351.6:p.Phe140Ser
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24860A>G
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.362T>C
  hgvsp: ENSP00000366142.3:p.Phe121Ser
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.419T>C
  hgvsp: ENSP00000380165.1:p.Phe140Ser
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Phe140Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

X-47837072-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837072
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837072
    reference: chr 0
allele count: 1
allele frequency: 1.152658029415833e-5
allele num: 86756
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.414T>A
  hgvsp: ENSP00000380165.1:p.His138Gln
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.357T>A
  hgvsp: ENSP00000366142.3:p.His119Gln
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24855A>T
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.414T>A
  hgvsp: ENSP00000306351.6:p.His138Gln
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1157
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hgvs: p.His138Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

X-47837073-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837073
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837073
    reference: chr 0
allele count: 1
allele frequency: 1.153482363254666e-5
allele num: 86694
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.356A>T
  hgvsp: ENSP00000366142.3:p.His119Leu
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.413A>T
  hgvsp: ENSP00000380165.1:p.His138Leu
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24854T>A
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.413A>T
  hgvsp: ENSP00000306351.6:p.His138Leu
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.His138Leu
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

X-47837082-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837082
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837082
    reference: chr 0
allele count: 3
allele frequency: 3.473186996387885e-5
allele num: 86376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.404G>A
  hgvsp: ENSP00000306351.6:p.Arg135His
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24845C>T
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.347G>A
  hgvsp: ENSP00000366142.3:p.Arg116His
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.404G>A
  hgvsp: ENSP00000380165.1:p.Arg135His
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 291
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1137
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg135His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

X-47837083-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837083
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837083
    reference: chr 0
allele count: 2
allele frequency: 2.319217032329885e-5
allele num: 86236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24844G>A
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.403C>T
  hgvsp: ENSP00000306351.6:p.Arg135Cys
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.403C>T
  hgvsp: ENSP00000380165.1:p.Arg135Cys
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.346C>T
  hgvsp: ENSP00000366142.3:p.Arg116Cys
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 357
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  variant carriers: 0
hgvs: p.Arg135Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP

X-47837091-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837091
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837091
    reference: chr 0
allele count: 3
allele frequency: 3.504836674610963e-5
allele num: 85596
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.395A>G
  hgvsp: ENSP00000380165.1:p.Lys132Arg
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24836T>C
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.338A>G
  hgvsp: ENSP00000366142.3:p.Lys113Arg
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.395A>G
  hgvsp: ENSP00000306351.6:p.Lys132Arg
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Lys132Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

X-47837094-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837094
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837094
    reference: chr 0
allele count: 1
allele frequency: 1.16916673486806e-5
allele num: 85531
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.392C>G
  hgvsp: ENSP00000380165.1:p.Thr131Ser
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.392C>G
  hgvsp: ENSP00000306351.6:p.Thr131Ser
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.335C>G
  hgvsp: ENSP00000366142.3:p.Thr112Ser
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24833G>C
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Thr131Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

X-47837112-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837112
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837112
    reference: chr 0
allele count: 11
allele frequency: 1.310662837942498e-4
allele num: 83927
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.317A>G
  hgvsp: ENSP00000366142.3:p.Asp106Gly
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.374A>G
  hgvsp: ENSP00000380165.1:p.Asp125Gly
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24815T>C
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.374A>G
  hgvsp: ENSP00000306351.6:p.Asp125Gly
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 5715
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp125Gly
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD

X-47837131-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837131
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837131
    reference: chr 0
allele count: 1
allele frequency: 1.234019448146503e-5
allele num: 81036
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24796T>G
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.355A>C
  hgvsp: ENSP00000380165.1:p.Met119Leu
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.355A>C
  hgvsp: ENSP00000306351.6:p.Met119Leu
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.298A>C
  hgvsp: ENSP00000366142.3:p.Met100Leu
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Met119Leu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

X-47837134-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837134
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837134
    reference: chr 0
allele count: 1
allele frequency: 1.239495277522993e-5
allele num: 80678
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.295C>T
  hgvsp: ENST00000376943.3:c.295C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.352C>T
  hgvsp: ENST00000305127.6:c.352C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24793G>A
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.352C>T
  hgvsp: ENST00000396965.1:c.352C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Leu118Leu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

X-47837146-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837146
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837146
    reference: chr 0
allele count: 1
allele frequency: 1.280032768838882e-5
allele num: 78123
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.283G>C
  hgvsp: ENSP00000366142.3:p.Asp95His
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.340G>C
  hgvsp: ENSP00000380165.1:p.Asp114His
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.340G>C
  hgvsp: ENSP00000306351.6:p.Asp114His
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24781C>G
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Asp114His
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

X-47837152-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837152
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837152
    reference: chr 0
allele count: 1
allele frequency: 1.293577388267253e-5
allele num: 77305
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.334G>C
  hgvsp: ENSP00000306351.6:p.Asp112His
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.277G>C
  hgvsp: ENSP00000366142.3:p.Asp93His
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.334G>C
  hgvsp: ENSP00000380165.1:p.Asp112His
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24775C>G
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4431
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp112His
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

X-47837156-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837156
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837156
    reference: chr 0
allele count: 1
allele frequency: 1.311699043771397e-5
allele num: 76237
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.273G>A
  hgvsp: ENST00000376943.3:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.330G>A
  hgvsp: ENST00000305127.6:c.330G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24771C>T
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.330G>A
  hgvsp: ENST00000396965.1:c.330G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Gln110Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

X-47837174-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837174
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837174
    reference: chr 0
allele count: 5
allele frequency: 6.872946707171232e-5
allele num: 72749
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.312G>T
  hgvsp: ENSP00000306351.6:p.Gln104His
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.255G>T
  hgvsp: ENSP00000366142.3:p.Gln85His
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24753C>A
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.312G>T
  hgvsp: ENSP00000380165.1:p.Gln104His
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Gln104His
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

X-47837187-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837187
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837187
    reference: chr 0
allele count: 1
allele frequency: 1.451905626134301e-5
allele num: 68875
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24740T>G
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.299A>C
  hgvsp: ENSP00000306351.6:p.Gln100Pro
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.242A>C
  hgvsp: ENSP00000366142.3:p.Gln81Pro
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.299A>C
  hgvsp: ENSP00000380165.1:p.Gln100Pro
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Gln100Pro
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

X-47837215-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837215
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837215
    reference: chr 0
allele count: 1
allele frequency: 1.700391089950689e-5
allele num: 58810
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.290-19T>G
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24712A>C
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.233-19T>G
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.290-19T>G
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

X-47837216-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837216
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837216
    reference: chr 0
allele count: 1
allele frequency: 1.702272533832667e-5
allele num: 58745
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.290-20T>G
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.233-20T>G
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.290-20T>G
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24711A>C
  variant of: http://identifiers.org/hgnc/13156
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

X-47837218-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837218
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837218
    reference: chr 0
allele count: 1
allele frequency: 1.738344400792685e-5
allele num: 57526
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24709C>T
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.290-22G>A
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.233-22G>A
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.290-22G>A
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff

X-47837237-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837237
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837237
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 48666
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.290-41A>G
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.233-41A>G
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24690T>C
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.290-41A>G
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP

X-47837240-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837240
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837240
    reference: chr 0
allele count: 1
allele frequency: 2.121025728042081e-5
allele num: 47147
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.233-44C>T
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24687G>A
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.290-44C>T
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
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  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.290-44C>T
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
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site quality: DP
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site quality: FS
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site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

X-47837244-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837244
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837244
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 44326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24683C>T
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.233-48G>A
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.290-48G>A
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.290-48G>A
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

X-47837245-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047837245
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047837245
    reference: chr 0
allele count: 2
allele frequency: 4.598652594789726e-5
allele num: 43491
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.290-49C>T
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.290-49C>T
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-24682G>A
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.233-49C>T
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

X-47842301-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047842301
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047842301
    reference: chr 0
allele count: 3
allele frequency: 3.584272213527043e-5
allele num: 83699
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.289+48A>G
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.232+48A>G
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-19626T>C
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.289+48A>G
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1251
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
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site quality: BaseQRankSum

X-47842304-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047842304
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047842304
    reference: chr 0
allele count: 1
allele frequency: 1.195257219353605e-5
allele num: 83664
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.232+45C>A
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.289+45C>A
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-19623G>T
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.289+45C>A
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

X-47842307-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047842307
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047842307
    reference: chr 0
allele count: 1
allele frequency: 1.194200960137572e-5
allele num: 83738
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.232+42C>T
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.289+42C>T
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-19620G>A
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.289+42C>T
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7840
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9381
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4285
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1714
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2112
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7995
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3828
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2243
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1588
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4641
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2809
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3976
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3087
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15429
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

X-47842316-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047842316
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047842316
    reference: chr 0
allele count: 3
allele frequency: 3.570408454727221e-5
allele num: 84024
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-19611T>C
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.289+33A>G
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.289+33A>G
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.232+33A>G
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7972
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6536
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3836
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3534
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3267
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1484
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2004
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2821
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1271
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8001
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4804
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2334
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

X-47842323-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24047842323
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24047842323
    reference: chr 0
allele count: 4
allele frequency: 4.73507268336569e-5
allele num: 84476
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000366142
  ensembl transcript: ENST00000376943
  gene symbol: ZNF182
  hgvsc: ENST00000376943.3:c.232+26T>C
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197779
  ensembl protein: ENSP00000366149
  ensembl transcript: ENST00000376950
  gene symbol: ZNF81
  hgvsc: ENST00000376950.4:c.278-19604A>G
  variant of: http://identifiers.org/hgnc/13156
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000380165
  ensembl transcript: ENST00000396965
  gene symbol: ZNF182
  hgvsc: ENST00000396965.1:c.289+26T>C
  variant of: http://identifiers.org/hgnc/13001
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147118
  ensembl protein: ENSP00000306351
  ensembl transcript: ENST00000305127
  gene symbol: ZNF182
  hgvsc: ENST00000305127.6:c.289+26T>C
  variant of: http://identifiers.org/hgnc/13001
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 111
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1165
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9264
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 9.18800964741013e-4
allele num: 8707
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47503
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6626
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.57e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.493e0

FS
type: SiteQuality
SIO_000300: 6.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.607e1

DP
type: SiteQuality
SIO_000300: 1.549787e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e0

GenotypeQuality
all individuals: 6378
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1368
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9260
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8487
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8721
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.104377104377104e-5
allele num: 47520
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 611
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

FS
type: SiteQuality
SIO_000300: 2.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

DP
type: SiteQuality
SIO_000300: 1.549832e6

QD
type: SiteQuality
SIO_000300: 1.428e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.319e0

GenotypeQuality
all individuals: 356
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1366
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1316
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6625
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.103713053539497e-5
allele num: 47535
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8485
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.942e1

QD
type: SiteQuality
SIO_000300: 1.544e1

DP
type: SiteQuality
SIO_000300: 1.551078e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.314e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

FS
type: SiteQuality
SIO_000300: 9.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.38e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.68e-1

GenotypeQuality
all individuals: 546
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 9.25e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6628
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.631321370309951e-3
allele num: 613
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9269
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 1.584427342689e-3
allele num: 8836
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 2.103491796381994e-4
allele num: 47540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.553934e6

MQRankSum
type: SiteQuality
SIO_000300: 4.56e-1

QD
type: SiteQuality
SIO_000300: 1.976e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.936e0

FS
type: SiteQuality
SIO_000300: 5.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.494e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.33e0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1164
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6627
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.20601038884566e-5
allele num: 47551
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8949
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9263
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.559037e6

MQRankSum
type: SiteQuality
SIO_000300: -5.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.261e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.69e-2

FS
type: SiteQuality
SIO_000300: 2.4762e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.45e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
SIO_000300: 2.688e1

GenotypeQuality
all individuals: 199
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1163
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46191
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9266
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8473
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.10017851517379e-5
allele num: 47615
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9135
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.704e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.565522e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.92e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.03e0

QD
type: SiteQuality
SIO_000300: 2.964e1

GenotypeQuality
all individuals: 316
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1291
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 560
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.08991825613079e-4
allele num: 9175
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47622
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9266
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6628
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.567114e6

QD
type: SiteQuality
SIO_000300: 3.252e1

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.63e-2

MQ
type: SiteQuality
SIO_000300: 5.958e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 194
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1290
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1160
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 625
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.097139501719654e-5
allele num: 47684
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6629
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.184834123222749e-4
allele num: 8440
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9274
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9403
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

DP
type: SiteQuality
SIO_000300: 1.573578e6

FS
type: SiteQuality
SIO_000300: 2.605e0

VQSLOD
type: SiteQuality
SIO_000300: -4.09e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

QD
type: SiteQuality
SIO_000300: 7.6e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeQuality
all individuals: 108
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6426
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 9.25e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 3.356408642752255e-4
allele num: 47670
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.063603488619443e-4
allele num: 9402
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.185395922238028e-4
allele num: 8436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 625
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6624
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.235198964736332e-4
allele num: 9273
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.574285e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 5.75e0

MQRankSum
type: SiteQuality
SIO_000300: 5.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.223e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.47e-1

QD
type: SiteQuality
SIO_000300: 1.78e1

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6413
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9242
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47636
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.078515962036238e-4
allele num: 9272
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.61e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.266e0

DP
type: SiteQuality
SIO_000300: 1.56131e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.38e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.233e0

QD
type: SiteQuality
SIO_000300: 3.135e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

GenotypeQuality
all individuals: 197
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1155
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47594
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.079097874177188e-4
allele num: 9267
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8427
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9023
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.203e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 1.552126e6

FS
type: SiteQuality
SIO_000300: 4.064e0

MQRankSum
type: SiteQuality
SIO_000300: -1.047e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.676e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

GenotypeQuality
all individuals: 222
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1276
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 141
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6631
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8918
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.07863229425089e-4
allele num: 9271
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 9.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.955e1

FS
type: SiteQuality
SIO_000300: 3.268e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.003e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.25e0

DP
type: SiteQuality
SIO_000300: 1.549072e6

QD
type: SiteQuality
SIO_000300: 1.488e1

GenotypeQuality
all individuals: 1153
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8894
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.103447550535327e-5
allele num: 47541
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6631
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8441
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9270
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.657e1

VQSLOD
type: SiteQuality
SIO_000300: -1.001e0

MQ
type: SiteQuality
SIO_000300: 5.837e1

FS
type: SiteQuality
SIO_000300: 4.122e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.337e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.36e-1

DP
type: SiteQuality
SIO_000300: 1.549115e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

GenotypeQuality
all individuals: 1328
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6336
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 19
allele frequency: 4.199823165340406e-3
allele num: 4524
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.183572020357439e-4
allele num: 8449
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8859
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 619
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 118
allele frequency: 2.482590309482233e-3
allele num: 47531
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6631
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 4.314529177003559e-4
allele num: 9271
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.16e0

MQRankSum
type: SiteQuality
SIO_000300: 2.91e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: 1.998e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.83e-1

DP
type: SiteQuality
SIO_000300: 1.555831e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.91e-1

QD
type: SiteQuality
SIO_000300: 1.951e1

GenotypeQuality
all individuals: 45019
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2141
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47551
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8892
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.549035845262037e-4
allele num: 8453
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4523
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9276
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.549367e6

VQSLOD
type: SiteQuality
SIO_000300: -1.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.73e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

QD
type: SiteQuality
SIO_000300: 1.857e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.65e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

FS
type: SiteQuality
SIO_000300: 5.22e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

GenotypeQuality
all individuals: 45119
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8884
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6631
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8451
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.103093650760269e-5
allele num: 47549
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 619
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.014e1

QD
type: SiteQuality
SIO_000300: 1.458e1

MQRankSum
type: SiteQuality
SIO_000300: 2.33e0

VQSLOD
type: SiteQuality
SIO_000300: 9.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.459e0

DP
type: SiteQuality
SIO_000300: 1.549964e6

FS
type: SiteQuality
SIO_000300: 9.816000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.16e0

GenotypeQuality
all individuals: 1231
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 45593
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8983
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.102076851929706e-5
allele num: 47572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 619
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9273
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4523
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.952e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.5e-1

DP
type: SiteQuality
SIO_000300: 1.555575e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -9.84e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.059e-1

MQ
type: SiteQuality
SIO_000300: 5.882e1

FS
type: SiteQuality
SIO_000300: 1.941e0

QD
type: SiteQuality
SIO_000300: 1.181e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.72e-1

GenotypeQuality
all individuals: 553
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46072
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9129
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8467
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 619
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4523
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9271
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.015226895823911e-4
allele num: 6633
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47613
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.560273e6

MQRankSum
type: SiteQuality
SIO_000300: 3.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.67e0

FS
type: SiteQuality
SIO_000300: 4.907e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.98e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 1.734e1

VQSLOD
type: SiteQuality
SIO_000300: -1.663e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.26e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.52e-1

GenotypeQuality
all individuals: 1352
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6431
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.179941002949853e-4
allele num: 8475
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 619
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4521
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47691
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9464
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e0

DP
type: SiteQuality
SIO_000300: 1.573274e6

FS
type: SiteQuality
SIO_000300: 6.403e0

QD
type: SiteQuality
SIO_000300: 1.156e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
type: SiteQuality
SIO_000300: 4.39e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

GenotypeQuality
all individuals: 218
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9275
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 619
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47691
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6634
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4521
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.359882005899705e-4
allele num: 8475
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9459
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.071e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.04e-1

DP
type: SiteQuality
SIO_000300: 1.574065e6

FS
type: SiteQuality
SIO_000300: 1.769e0

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.580000000000001e-1

GenotypeQuality
all individuals: 1163
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1352
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9270
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9511
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.0965239632689e-5
allele num: 47698
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8475
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4522
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 1.329e1

MQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.99e1

VQSLOD
type: SiteQuality
SIO_000300: 3.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.91e-1

DP
type: SiteQuality
SIO_000300: 1.575358e6

GenotypeQuality
all individuals: 6435
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1354
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1171
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4521
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.095381778560054e-5
allele num: 47724
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9617
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9272
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8479
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.924e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e0

DP
type: SiteQuality
SIO_000300: 1.577909e6

VQSLOD
type: SiteQuality
SIO_000300: 5.679999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.4e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.175e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

GenotypeQuality
all individuals: 6399
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 209
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47564
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.283380458686774e-5
allele num: 47745
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9785
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.597444089456869e-3
allele num: 626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9262
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 25
allele frequency: 5.533421868083223e-3
allele num: 4518
num of homozygotes: 1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.263e0

FS
type: SiteQuality
SIO_000300: 5.25e-1

QD
type: SiteQuality
SIO_000300: 1.971e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.57e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
SIO_000300: 1.381e1

MQRankSum
type: SiteQuality
SIO_000300: 3.88e-1

DP
type: SiteQuality
SIO_000300: 1.581122e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.136e-1

GenotypeQuality
all individuals: 177
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6400
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47747
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 4.076640847941296e-4
allele num: 9812
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9262
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 627
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.486e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.54e-1

DP
type: SiteQuality
SIO_000300: 1.580065e6

MQRankSum
type: SiteQuality
SIO_000300: -3.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

GenotypeQuality
all individuals: 1159
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 627
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4517
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9830
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9257
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.095162270317836e-5
allele num: 47729
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6623
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.62e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-2

DP
type: SiteQuality
SIO_000300: 1.579091e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.298e0

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.96e0

QD
type: SiteQuality
SIO_000300: 1.508e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeQuality
all individuals: 1215
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 6369
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9830
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6623
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9257
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 627
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 4.427717511622758e-4
allele num: 4517
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.179245283018868e-4
allele num: 8480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 2.514194724381403e-4
allele num: 47729
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

DP
type: SiteQuality
SIO_000300: 1.579091e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.62e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.298e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 5.96e0

QD
type: SiteQuality
SIO_000300: 1.508e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 213
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1334
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.179662616491683e-4
allele num: 8477
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9833
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9256
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47726
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6624
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.109e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.178e0

VQSLOD
type: SiteQuality
SIO_000300: -3.211e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.07e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.32e-1

QD
type: SiteQuality
SIO_000300: 3.222e1

DP
type: SiteQuality
SIO_000300: 1.577671e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e-1

GenotypeQuality
all individuals: 1209
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 971
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9258
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.597444089456869e-3
allele num: 626
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 6.037735849056604e-4
allele num: 6625
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4514
num of homozygotes: 0

African
type: Population
allele count: 14
allele frequency: 1.651917404129794e-3
allele num: 8475
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.017811704834606e-4
allele num: 9825
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47717
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.129e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.77e-1

QD
type: SiteQuality
SIO_000300: 1.615e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.76e-2

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: 3.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e-1

DP
type: SiteQuality
SIO_000300: 1.5763e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e-1

GenotypeQuality
all individuals: 1193
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6270
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47218
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9255
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 625
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8475
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.096040579345616e-5
allele num: 47709
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9837
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6624
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.5e-1

QD
type: SiteQuality
SIO_000300: 1.636e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

DP
type: SiteQuality
SIO_000300: 1.57339e6

MQRankSum
type: SiteQuality
SIO_000300: 5.91e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.252e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.094e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
all individuals: 84
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2184
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6621
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8463
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.215820961666297e-4
allele num: 4513
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47511
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9632
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.95e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 1.531921e6

FS
type: SiteQuality
SIO_000300: 3.398e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e-1

QD
type: SiteQuality
SIO_000300: 1.455e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e0

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: -3.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

GenotypeQuality
all individuals: 1047
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40648
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1341
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9233
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4509
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6617
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9537
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.323644105309753e-5
allele num: 47441
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 621
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.78e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.041e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

MQRankSum
type: SiteQuality
SIO_000300: 6.94e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.22e0

QD
type: SiteQuality
SIO_000300: 3.184e1

MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
SIO_000300: 1.505741e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

GenotypeQuality
all individuals: 1161
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2777
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6613
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.084481075805227e-4
allele num: 9221
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4507
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8452
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9453
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47390
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

VQSLOD
type: SiteQuality
SIO_000300: -4.075e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 1.498551e6

MQ
type: SiteQuality
SIO_000300: 5.83e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.348e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.02e-2

QD
type: SiteQuality
SIO_000300: 3.081e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

GenotypeQuality
all individuals: 959
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.338474540460596e-5
allele num: 47330
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9219
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 619
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6611
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9328
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8443
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4509
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.823e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.92e0

MQRankSum
type: SiteQuality
SIO_000300: 3.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.096e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.070000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.481514e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.23e-2

FS
type: SiteQuality
SIO_000300: 7.178e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e-1

GenotypeQuality
all individuals: 493
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38702
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 1.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9217
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9230
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.028467595396729e-4
allele num: 6604
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47296
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

VQSLOD
type: SiteQuality
SIO_000300: 7.69e-1

FS
type: SiteQuality
SIO_000300: 6.272e0

QD
type: SiteQuality
SIO_000300: 1.251e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.872e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

DP
type: SiteQuality
SIO_000300: 1.478046e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.34e-1

GenotypeQuality
all individuals: 1121
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5370
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1335
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6605
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.114164904862579e-5
allele num: 47300
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8438
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9216
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9249
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4507
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.036e0

FS
type: SiteQuality
SIO_000300: 2.943e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

QD
type: SiteQuality
SIO_000300: 1.375e1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 1.47746e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e-1

GenotypeQuality
all individuals: 1183
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2067
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5353
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9215
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8435
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.113718030014796e-5
allele num: 47310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9219
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6603
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.478384e6

MQ
type: SiteQuality
SIO_000300: 5.906e1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.44e-2

GenotypeQuality
all individuals: 980
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5264
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47333
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9201
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9219
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.371072910491998e-4
allele num: 8435
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4509
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.78e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.262e0

FS
type: SiteQuality
SIO_000300: 1.0495e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-1

DP
type: SiteQuality
SIO_000300: 1.489153e6

QD
type: SiteQuality
SIO_000300: 2.592e1

GenotypeQuality
all individuals: 42999
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5321
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 9.25e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 613
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47370
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4509
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9184
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9221
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.159999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.48e-2

QD
type: SiteQuality
SIO_000300: 3.325e1

DP
type: SiteQuality
SIO_000300: 1.501679e6

GenotypeQuality
all individuals: 158
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 5323
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1109
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.084245906971701e-4
allele num: 9223
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.089561996077577e-4
allele num: 9178
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.53864362646467e-3
allele num: 8449
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 615
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47361
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4509
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6611
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.943e1

DP
type: SiteQuality
SIO_000300: 1.50369e6

MQRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.99e-2

QD
type: SiteQuality
SIO_000300: 1.525e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.814e0

VQSLOD
type: SiteQuality
SIO_000300: 8.55e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.48e-1

GenotypeQuality
all individuals: 1006
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
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variant carriers: 0

GenotypeQuality
all individuals: 1177
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6618
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.08283703302653e-4
allele num: 9235
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9230
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8451
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47453
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4510
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.776e0

QD
type: SiteQuality
SIO_000300: 1.932e1

DP
type: SiteQuality
SIO_000300: 1.517093e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.39e-1

GenotypeQuality
all individuals: 45419
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 2.75e1
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GenotypeQuality
all individuals: 496
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 174
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8461
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.074113856068743e-4
allele num: 9310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4513
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9233
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6624
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.785e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.77e-2

DP
type: SiteQuality
SIO_000300: 1.52436e6

VQSLOD
type: SiteQuality
SIO_000300: 1.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 45796
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 9.25e1
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GenotypeQuality
all individuals: 631
bin: 2.75e1
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GenotypeQuality
all individuals: 310
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8465
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.075268817204301e-4
allele num: 9300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4515
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6625
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.0e-3

FS
type: SiteQuality
SIO_000300: 8.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-1

DP
type: SiteQuality
SIO_000300: 1.528692e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

QD
type: SiteQuality
SIO_000300: 8.960000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -3.972e-1

GenotypeQuality
all individuals: 1003
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 3.25e1
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GenotypeQuality
all individuals: 1176
bin: 9.75e1
variant carriers: 5

East Asian
type: Population
allele count: 1
allele frequency: 1.508750754375377e-4
allele num: 6628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 8.41467519353753e-5
allele num: 47536
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9237
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9345
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.21483942414175e-4
allele num: 4515
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8469
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.258e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.38e-1

QD
type: SiteQuality
SIO_000300: 1.384e1

DP
type: SiteQuality
SIO_000300: 1.530751e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.75e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 8.35e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.086e-1

GenotypeQuality
all individuals: 1141
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6628
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9399
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47587
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4519
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9239
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.724e0

DP
type: SiteQuality
SIO_000300: 1.541355e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.78e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.88e-1

QD
type: SiteQuality
SIO_000300: 3.231e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.896e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

GenotypeQuality
all individuals: 1013
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 506
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.30159430335875e-5
allele num: 47607
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.164970772894566e-4
allele num: 9238
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 8.468296813803324e-4
allele num: 9447
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6628
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-2

DP
type: SiteQuality
SIO_000300: 1.542845e6

FS
type: SiteQuality
SIO_000300: 2.509e0

VQSLOD
type: SiteQuality
SIO_000300: 5.02e0

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.015e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

QD
type: SiteQuality
SIO_000300: 1.981e1

GenotypeQuality
all individuals: 1027
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 619
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8485
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9240
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9485
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.099164532516059e-5
allele num: 47638
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6628
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.57e-1

QD
type: SiteQuality
SIO_000300: 1.364e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.08e0

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

MQ
type: SiteQuality
SIO_000300: 5.975e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.03e0

DP
type: SiteQuality
SIO_000300: 1.545643e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

GenotypeQuality
all individuals: 512
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5711
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9251
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8499
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6633
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9674
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.191114836546522e-5
allele num: 47720
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.72e0

DP
type: SiteQuality
SIO_000300: 1.558573e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.32e-1

QD
type: SiteQuality
SIO_000300: 1.153e1

FS
type: SiteQuality
SIO_000300: 1.1086e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.28e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

VQSLOD
type: SiteQuality
SIO_000300: -1.398e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.19e-1

GenotypeQuality
all individuals: 1170
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 108
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47728
num of homozygotes: 0

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

East Asian
type: Population
allele count: 4
allele frequency: 6.031363088057901e-4
allele num: 6632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9248
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9738
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 623
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4521
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.54e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.304e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e-1

QD
type: SiteQuality
SIO_000300: 1.743e1

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.204e0

DP
type: SiteQuality
SIO_000300: 1.562833e6

GenotypeQuality
all individuals: 1172
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 119
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47685
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9720
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4515
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6628
num of homozygotes: 0

African
type: Population
allele count: 14
allele frequency: 1.647446457990115e-3
allele num: 8498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 623
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.163331530557058e-4
allele num: 9245
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-2

DP
type: SiteQuality
SIO_000300: 1.561309e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.483e0

FS
type: SiteQuality
SIO_000300: 1.76e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

QD
type: SiteQuality
SIO_000300: 1.461e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

GenotypeQuality
all individuals: 182
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9699
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.098283604011918e-5
allele num: 47658
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8495
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9238
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6628
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.07e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-2

DP
type: SiteQuality
SIO_000300: 1.557934e6

QD
type: SiteQuality
SIO_000300: 3.43e1

GenotypeQuality
all individuals: 48321
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9237
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4511
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.508978421608571e-4
allele num: 6627
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8489
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9665
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47605
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.82e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.26e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 1.31e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

DP
type: SiteQuality
SIO_000300: 1.55535e6

GenotypeQuality
all individuals: 998
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1156
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1155
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48130
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8489
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6625
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9233
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 621
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.101855938793955e-5
allele num: 47577
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9639
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.01e0

MQRankSum
type: SiteQuality
SIO_000300: -6.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.002e0

DP
type: SiteQuality
SIO_000300: 1.553909e6

QD
type: SiteQuality
SIO_000300: 9.34e0

GenotypeQuality
all individuals: 274
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47279
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2028
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47414
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4505
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6619
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.53898784947505e-4
allele num: 8477
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.124e0

DP
type: SiteQuality
SIO_000300: 1.544641e6

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.31e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.88e-1

QD
type: SiteQuality
SIO_000300: 1.524e1

GenotypeQuality
all individuals: 986
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
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variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1156
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 1
allele frequency: 1.084951719648476e-4
allele num: 9217
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6618
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.056524035921817e-4
allele num: 9465
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47350
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4497
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 615
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.825e1

VQSLOD
type: SiteQuality
SIO_000300: -2.51e0

MQRankSum
type: SiteQuality
SIO_000300: -2.503e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.05e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.812e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.32e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.540941e6

GenotypeQuality
all individuals: 5398
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 642
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.373215499660095e-5
allele num: 47072
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9193
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6601
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8452
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.59e-2

MQ
type: SiteQuality
SIO_000300: 5.938e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.3e-1

FS
type: SiteQuality
SIO_000300: 1.007e0

VQSLOD
type: SiteQuality
SIO_000300: -2.784e0

QD
type: SiteQuality
SIO_000300: 2.732e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e-1

DP
type: SiteQuality
SIO_000300: 1.520493e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQRankSum
type: SiteQuality
SIO_000300: 9.04e-1

GenotypeQuality
all individuals: 162
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1094
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1154
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47035
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.183852255238546e-4
allele num: 8447
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 613
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4486
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.9033e1

MQRankSum
type: SiteQuality
SIO_000300: 5.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.623e0

DP
type: SiteQuality
SIO_000300: 1.517558e6

QD
type: SiteQuality
SIO_000300: 1.296e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.78e-1

GenotypeQuality
all individuals: 971
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 484
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variant carriers: 0

GenotypeQuality
all individuals: 1159
bin: 9.75e1
variant carriers: 11

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.191753068764152e-3
allele num: 8391
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4457
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46319
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8479
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.095890410958904e-4
allele num: 9125
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.27e0

FS
type: SiteQuality
SIO_000300: 5.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.32e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.85e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.15e-1

DP
type: SiteQuality
SIO_000300: 1.47017e6

QD
type: SiteQuality
SIO_000300: 1.857e1

GenotypeQuality
all individuals: 206
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
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variant carriers: 0

GenotypeQuality
all individuals: 471
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variant carriers: 0

GenotypeQuality
all individuals: 4765
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 575
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44961
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.108647450110865e-4
allele num: 9020
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7346
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.63e0

DP
type: SiteQuality
SIO_000300: 1.406551e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e0

QD
type: SiteQuality
SIO_000300: 1.342e1

VQSLOD
type: SiteQuality
SIO_000300: 5.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.72e-1

FS
type: SiteQuality
SIO_000300: 3.227e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 159
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 986
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variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6457
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.232192682872385e-5
allele num: 44799
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8295
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8998
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4353
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.635e-1

DP
type: SiteQuality
SIO_000300: 1.398672e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.143e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

GenotypeQuality
all individuals: 879
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4509
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.129177958446251e-4
allele num: 8856
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6372
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6352
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4265
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43530
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.779e1

DP
type: SiteQuality
SIO_000300: 1.343593e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.068e0

QD
type: SiteQuality
SIO_000300: 1.082e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.39e-1

FS
type: SiteQuality
SIO_000300: 2.671e0

VQSLOD
type: SiteQuality
SIO_000300: -1.654e0

MQRankSum
type: SiteQuality
SIO_000300: 7.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.2e-1

GenotypeQuality
all individuals: 863
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1136
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 738
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.224889759921607e-4
allele num: 8164
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6144
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6308
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43099
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8813
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 542
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4235
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.849e1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.497e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.01e-1

DP
type: SiteQuality
SIO_000300: 1.326429e6

QD
type: SiteQuality
SIO_000300: 5.66e0

GenotypeQuality
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1135
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 373
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4284
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8735
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.351502610167897e-5
allele num: 42526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8111
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5879
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.86e0

QD
type: SiteQuality
SIO_000300: 5.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.012e0

VQSLOD
type: SiteQuality
SIO_000300: -2.912e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

FS
type: SiteQuality
SIO_000300: 9.74e-1

DP
type: SiteQuality
SIO_000300: 1.302876e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.263e0

MQ
type: SiteQuality
SIO_000300: 6.014e1

GenotypeQuality
all individuals: 370
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 149
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1126
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 191
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5165
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7934
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40613
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8476
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 8.279516476237788e-4
allele num: 6039
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4013
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 509
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.266e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.225183e6

QD
type: SiteQuality
SIO_000300: 1.625e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

GenotypeQuality
all individuals: 1611
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24573
bin: 6.25e1
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GenotypeQuality
all individuals: 230
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7720
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4625
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.60586319218241e-5
allele num: 38375
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3816
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5747
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8121
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 471
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.128018e6

MQRankSum
type: SiteQuality
SIO_000300: 1.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.391e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.72e0

VQSLOD
type: SiteQuality
SIO_000300: -9.147999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

FS
type: SiteQuality
SIO_000300: 3.634e0

QD
type: SiteQuality
SIO_000300: 1.515e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.8e-3

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 1.25e1
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GenotypeQuality
all individuals: 265
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3438
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4931
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.070498648980594e-5
allele num: 32568
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7105
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.686e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.15e-2

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.072e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.41e0

VQSLOD
type: SiteQuality
SIO_000300: -1.771e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

DP
type: SiteQuality
SIO_000300: 8.52116e5

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
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variant carriers: 0

GenotypeQuality
all individuals: 1607
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3425
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.409046075806679e-4
allele num: 7097
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7062
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3287
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4930
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.144e1

DP
type: SiteQuality
SIO_000300: 8.5154e5

VQSLOD
type: SiteQuality
SIO_000300: 9.1e-1

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.24e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

GenotypeQuality
all individuals: 9220
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1424
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6989
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3304
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.433897332950961e-4
allele num: 6974
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31805
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4830
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.04e-1

DP
type: SiteQuality
SIO_000300: 8.18266e5

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.588e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.34e-2

GenotypeQuality
all individuals: 228
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2540
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2749
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6076
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6312
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4056
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26593
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 340
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.24e-2

DP
type: SiteQuality
SIO_000300: 6.68033e5

GenotypeQuality
all individuals: 1100
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 356
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25678
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3906
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2473
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.705320600272851e-4
allele num: 5864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2682
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.626e-1

DP
type: SiteQuality
SIO_000300: 6.57662e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.42e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.087e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.34e-1

QD
type: SiteQuality
SIO_000300: 1.64e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.06e-1

GenotypeQuality
all individuals: 167
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3587
bin: 2.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24123
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5890
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 315
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2322
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.48e1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: 5.36e-1

DP
type: SiteQuality
SIO_000300: 6.4513e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.62e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 117
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1460
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2528
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5811
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3554
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.872308556450103e-4
allele num: 5341
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.226006846131091e-5
allele num: 23663
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.585e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.63e-2

QD
type: SiteQuality
SIO_000300: 1.737e1

MQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

DP
type: SiteQuality
SIO_000300: 6.4249e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.47e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2246
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2004
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 599
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9009
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4397
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.202212070209185e-4
allele num: 8318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45920
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9059
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.126465530717524e-4
allele num: 6397
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.804e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

DP
type: SiteQuality
SIO_000300: 1.597376e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.79e-1

QD
type: SiteQuality
SIO_000300: 1.338e1

MQRankSum
type: SiteQuality
SIO_000300: -8.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.0e0

GenotypeQuality
all individuals: 2279
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1708
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1262
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9010
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9062
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4397
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8322
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 599
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.179029024666609e-5
allele num: 45892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6382
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.335e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.11e-2

QD
type: SiteQuality
SIO_000300: 1.302e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.149999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.26e-1

DP
type: SiteQuality
SIO_000300: 1.605796e6

GenotypeQuality
all individuals: 2322
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1984
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1265
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 599
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.10265740434447e-4
allele num: 9069
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9019
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4400
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8317
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45926
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.647e0

DP
type: SiteQuality
SIO_000300: 1.61521e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.084e-1

GenotypeQuality
all individuals: 1273
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1725
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20764
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.169291509393032e-5
allele num: 46098
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 599
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.211655424084928e-4
allele num: 9043
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9125
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6423
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8330
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.499000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -1.181e0

DP
type: SiteQuality
SIO_000300: 1.652491e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.09e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQRankSum
type: SiteQuality
SIO_000300: 4.55e-1

QD
type: SiteQuality
SIO_000300: 2.009e1