X-119669741-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119669741
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119669741
    reference: chr 0
allele count: 612
allele frequency: 7.312701636993667e-3
allele num: 83690
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.2104A>G
  hgvsp: ENSP00000360373.5:p.Lys702Glu
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.590A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.2119A>G
  hgvsp: ENSP00000338919.6:p.Lys707Glu
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.2158A>G
  hgvsp: ENSP00000384109.3:p.Lys720Glu
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 11654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 8.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4377
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 6.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 7.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 3862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15346
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4226
  bin: 9.75e1
  variant carriers: 927
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 8.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
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  variant carriers: 11
genotype quality: GenotypeQuality
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  variant carriers: 12
genotype quality: GenotypeQuality
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  variant carriers: 13
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 2778
  bin: 8.25e1
  variant carriers: 21
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 74
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  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 17100
  bin: 9.75e1
  variant carriers: 833
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 2361
  bin: 7.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 2456
  bin: 2.5e0
  variant carriers: 10
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 20435
  bin: 6.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 5
hgvs: p.Lys720Glu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

X-119669741-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119669741
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119669742
    reference: chr 0
allele count: 1
allele frequency: 1.194885888397658e-5
allele num: 83690
alternate allele: TC
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.2157dupG
  hgvsp: ENSP00000384109.3:p.Lys720GlufsTer18
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.2103dupG
  hgvsp: ENSP00000360373.5:p.Lys702GlufsTer18
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.2118dupG
  hgvsp: ENSP00000338919.6:p.Lys707GlufsTer18
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.589dupG
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
  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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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 17100
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genotype quality: GenotypeQuality
  all individuals: 1388
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys720GlufsTer18
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP

X-119669813-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119669813
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119669813
    reference: chr 0
allele count: 2
allele frequency: 2.293288690646822e-5
allele num: 87211
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.533-15T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.2101-15T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.2047-15T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.2062-15T>C
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 6.25e1
  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: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3871
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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: 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
  all individuals: 2937
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genotype quality: GenotypeQuality
  all individuals: 1440
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  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS

X-119669830-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119669830
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119669830
    reference: chr 0
allele count: 2
allele frequency: 2.301548942438261e-5
allele num: 86898
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.2047-32G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.2062-32G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.533-32G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.2101-32G>A
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 555
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
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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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  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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  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
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 2902
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD

X-119669834-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119669834
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119669834
    reference: chr 0
allele count: 2
allele frequency: 2.308269375036067e-5
allele num: 86645
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.533-36C>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.2101-36C>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.2062-36C>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.2047-36C>A
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9988
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 6.25e1
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genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  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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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 2853
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1664
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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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: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14817
  bin: 6.25e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-119669837-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119669837
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119669837
    reference: chr 0
allele count: 1
allele frequency: 1.152937107280798e-5
allele num: 86735
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.533-39A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.2062-39A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.2047-39A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.2101-39A>G
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 9.75e1
  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
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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: 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
  all individuals: 3843
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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: 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: 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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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13828
  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 8.75e1
  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
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2232
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2531
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

X-119669841-ATACCACATT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119669841
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119669832
    reference: chr 0
allele count: 1
allele frequency: 1.154907780613718e-5
allele num: 86587
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8946
  bin: 3.25e1
  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
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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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  variant carriers: 0
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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  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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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
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
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 1416
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: ATACCACATT
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ

X-119670747-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670747
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670747
    reference: chr 0
allele count: 4
allele frequency: 4.660049396523603e-5
allele num: 85836
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.2046+35T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.2100+35T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.2061+35T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.532+35T>C
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.25e1
  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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  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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  bin: 4.25e1
  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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  variant carriers: 1
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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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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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
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 836
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

X-119670750-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670750
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670750
    reference: chr 0
allele count: 5
allele frequency: 5.821535022354694e-5
allele num: 85888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.532+32G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.2100+32G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.2046+32G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.2061+32G>A
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 1
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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  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
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-119670753-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670753
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670754
    reference: chr 0
allele count: 1
allele frequency: 1.161696541629396e-5
allele num: 86081
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.532+28dupA
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.2100+28dupA
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.2061+28dupA
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.2046+28dupA
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 2.25e1
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

X-119670753-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670753
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670753
    reference: chr 0
allele count: 1
allele frequency: 1.161696541629396e-5
allele num: 86081
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.2046+29T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.532+29T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.2061+29T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.2100+29T>C
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  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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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
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genotype depth: GenotypeDepth
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  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

X-119670761-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670761
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670761
    reference: chr 0
allele count: 1
allele frequency: 1.155788768044752e-5
allele num: 86521
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.532+21C>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.2100+21C>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.2061+21C>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.2046+21C>G
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 1.25e1
  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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 1107
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

X-119670776-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670776
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670776
    reference: chr 0
allele count: 26
allele frequency: 2.981412042611258e-4
allele num: 87207
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.2061+6A>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.2100+6A>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.532+6A>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.2046+6A>C
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 6.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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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: 5.75e1
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genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.75e1
  variant carriers: 1
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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  bin: 4.75e1
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genotype depth: GenotypeDepth
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 8579
  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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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
hgvs: c.2100+6A>C
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

X-119670785-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670785
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670785
    reference: chr 0
allele count: 1
allele frequency: 1.144020775417282e-5
allele num: 87411
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.529A>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.2058A>T
  hgvsp: ENST00000336592.6:c.2058A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.2043A>T
  hgvsp: ENST00000371322.5:c.2043A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.2097A>T
  hgvsp: ENST00000404115.3:c.2097A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23737
  bin: 2.25e1
  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 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: 70
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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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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
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  variant carriers: 0
hgvs: p.Pro699Pro
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

X-119670789-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670789
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670789
    reference: chr 0
allele count: 1
allele frequency: 1.143183766790512e-5
allele num: 87475
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.2093C>T
  hgvsp: ENSP00000384109.3:p.Pro698Leu
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.2039C>T
  hgvsp: ENSP00000360373.5:p.Pro680Leu
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.2054C>T
  hgvsp: ENSP00000338919.6:p.Pro685Leu
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.525C>T
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
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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: 2831
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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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
  all individuals: 31
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  variant carriers: 0
hgvs: p.Pro698Leu
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

X-119670800-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670800
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670800
    reference: chr 0
allele count: 1
allele frequency: 1.141604639481255e-5
allele num: 87596
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.2043A>G
  hgvsp: ENST00000336592.6:c.2043A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.2028A>G
  hgvsp: ENST00000371322.5:c.2028A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.514A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.2082A>G
  hgvsp: ENST00000404115.3:c.2082A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  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 depth: GenotypeDepth
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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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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu694Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

X-119670805-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670805
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670805
    reference: chr 0
allele count: 4
allele frequency: 4.565063568510191e-5
allele num: 87622
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.509A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.2038A>G
  hgvsp: ENSP00000338919.6:p.Met680Val
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.2023A>G
  hgvsp: ENSP00000360373.5:p.Met675Val
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.2077A>G
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  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: missense
filter: PASS
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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hgvs: p.Met693Val
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ

X-119670818-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670818
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670818
    reference: chr 0
allele count: 2
allele frequency: 2.281516295730142e-5
allele num: 87661
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.2025G>A
  hgvsp: ENST00000336592.6:c.2025G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.2010G>A
  hgvsp: ENST00000371322.5:c.2010G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.496G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.2064G>A
  hgvsp: ENST00000404115.3:c.2064G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: synonymous
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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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.Pro688Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
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X-119670866-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670866
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670866
    reference: chr 0
allele count: 9
allele frequency: 1.028019235382138e-4
allele num: 87547
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1977G>A
  hgvsp: ENST00000336592.6:c.1977G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.448G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.2016G>A
  hgvsp: ENST00000404115.3:c.2016G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1962G>A
  hgvsp: ENST00000371322.5:c.1962G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8269
  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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hgvs: p.Pro672Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

X-119670892-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670892
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670892
    reference: chr 0
allele count: 2
allele frequency: 2.299299863191658e-5
allele num: 86983
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.425-3T>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1993-3T>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1939-3T>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1954-3T>A
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  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 quality: GenotypeQuality
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hgvs: c.1993-3T>A
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
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site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

X-119670898-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670898
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670898
    reference: chr 0
allele count: 1
allele frequency: 1.152618172178103e-5
allele num: 86759
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1993-9T>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.425-9T>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1954-9T>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1939-9T>G
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

X-119670908-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670908
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670908
    reference: chr 0
allele count: 15
allele frequency: 1.736774462468304e-4
allele num: 86367
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.425-19T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1939-19T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1993-19T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1954-19T>C
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
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X-119670914-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670914
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670914
    reference: chr 0
allele count: 1
allele frequency: 1.160671796836009e-5
allele num: 86157
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1993-25A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.425-25A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1954-25A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1939-25A>G
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  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 quality: GenotypeQuality
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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: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

X-119670934-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670934
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670934
    reference: chr 0
allele count: 1
allele frequency: 1.188848600130773e-5
allele num: 84115
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.425-45G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1939-45G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1993-45G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1954-45G>A
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10866
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum

X-119670939-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670939
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670939
    reference: chr 0
allele count: 2
allele frequency: 2.385923053981509e-5
allele num: 83825
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1954-50G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1939-50G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.425-50G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1993-50G>A
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 720
  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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  bin: 6.25e1
  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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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
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genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
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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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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5157
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1758
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2851
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1330
  bin: 1.75e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 3141
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3802
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

X-119670940-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119670940
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119670940
    reference: chr 0
allele count: 1
allele frequency: 1.197231999616886e-5
allele num: 83526
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1993-51T>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1939-51T>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.425-51T>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1954-51T>G
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
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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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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  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
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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: 0
genotype depth: GenotypeDepth
  all individuals: 515
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
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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
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genotype quality: GenotypeQuality
  all individuals: 4566
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5190
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  variant carriers: 1
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3651
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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: 2320
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1772
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ

X-119671927-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119671927
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119671927
    reference: chr 0
allele count: 6
allele frequency: 6.964111611495427e-5
allele num: 86156
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1938+52C>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1953+52C>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.424+52C>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1992+52C>G
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6811
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1602
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
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  variant carriers: 1
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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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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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1920
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1518
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2933
  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 6652
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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: 920
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

X-119671928-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119671928
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119671928
    reference: chr 0
allele count: 1
allele frequency: 1.159635410626899e-5
allele num: 86234
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.424+51T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1953+51T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1992+51T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1938+51T>C
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4568
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
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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: 360
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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: 5.25e1
  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: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.25e1
  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: 422
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3072
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
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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
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 2833
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

X-119671937-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119671937
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119671937
    reference: chr 0
allele count: 3
allele frequency: 3.477575434407132e-5
allele num: 86267
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.424+42A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1953+42A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1938+42A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1992+42A>G
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4091
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18548
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16162
  bin: 2.25e1
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 5214
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 1342
  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 1551
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

X-119671955-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119671955
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119671955
    reference: chr 0
allele count: 1
allele frequency: 1.154227936932986e-5
allele num: 86638
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.424+24T>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1992+24T>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1953+24T>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1938+24T>G
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
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genotype depth: GenotypeDepth
  all individuals: 422
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 2099
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 1772
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
reference allele: A
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

X-119671991-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119671991
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119671991
    reference: chr 0
allele count: 1
allele frequency: 1.14621062766494e-5
allele num: 87244
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1926T>C
  hgvsp: ENST00000371322.5:c.1926T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1941T>C
  hgvsp: ENST00000336592.6:c.1941T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1980T>C
  hgvsp: ENST00000404115.3:c.1980T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.412T>C
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
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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
  all individuals: 1800
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genotype quality: GenotypeQuality
  all individuals: 73
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  variant carriers: 0
hgvs: p.Ile660Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

X-119671997-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119671997
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119671997
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 87260
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1974C>A
  hgvsp: ENST00000404115.3:c.1974C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1935C>A
  hgvsp: ENST00000336592.6:c.1935C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.406C>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1920C>A
  hgvsp: ENST00000371322.5:c.1920C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
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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 depth: GenotypeDepth
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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
  all individuals: 912
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile658Ile
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: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ

X-119672018-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672018
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672018
    reference: chr 0
allele count: 3
allele frequency: 3.43957807842238e-5
allele num: 87220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1899C>T
  hgvsp: ENST00000371322.5:c.1899C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.385C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1953C>T
  hgvsp: ENST00000404115.3:c.1953C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1914C>T
  hgvsp: ENST00000336592.6:c.1914C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21212
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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
  all individuals: 167
  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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  bin: 6.25e1
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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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  bin: 6.75e1
  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
  all individuals: 267
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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
  all individuals: 72
  bin: 5.75e1
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 691
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genotype quality: GenotypeQuality
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  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 40315
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp651Asp
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

X-119672046-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672046
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672046
    reference: chr 0
allele count: 1
allele frequency: 1.154694410124361e-5
allele num: 86603
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1886C>T
  hgvsp: ENSP00000338919.6:p.Thr629Ile
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1871C>T
  hgvsp: ENSP00000360373.5:p.Thr624Ile
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.357C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1925C>T
  hgvsp: ENSP00000384109.3:p.Thr642Ile
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1120
  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 depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 1744
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 235
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genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr642Ile
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

X-119672060-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672060
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672060
    reference: chr 0
allele count: 179
allele frequency: 2.096288749136305e-3
allele num: 85389
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.343C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1872C>T
  hgvsp: ENST00000336592.6:c.1872C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1911C>T
  hgvsp: ENST00000404115.3:c.1911C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1857C>T
  hgvsp: ENST00000371322.5:c.1857C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
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  variant carriers: 21
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 129
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 2
genotype quality: GenotypeQuality
  all individuals: 121
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  variant carriers: 3
hgvs: p.Cys637Cys
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

X-119672083-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672083
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672083
    reference: chr 0
allele count: 6
allele frequency: 7.313773053622146e-5
allele num: 82037
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1853-19G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.320G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1868-19G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1907-19G>A
  variant of: http://identifiers.org/hgnc/2555
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
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  variant carriers: 1
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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  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
  all individuals: 2899
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genotype quality: GenotypeQuality
  all individuals: 1405
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

X-119672085-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672085
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672085
    reference: chr 0
allele count: 2
allele frequency: 2.450650034921763e-5
allele num: 81611
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1907-21A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.318A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1853-21A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1868-21A>G
  variant of: http://identifiers.org/hgnc/2555
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4965
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13038
  bin: 1.25e1
  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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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  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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  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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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 122
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5008
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3430
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5139
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1376
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

X-119672089-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672089
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672089
    reference: chr 0
allele count: 2
allele frequency: 2.469135802469136e-5
allele num: 81000
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1907-25A>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.314A>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1868-25A>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1853-25A>C
  variant of: http://identifiers.org/hgnc/2555
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14656
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  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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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
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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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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
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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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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
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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  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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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5137
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

X-119672090-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672090
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672090
    reference: chr 0
allele count: 3
allele frequency: 3.707182047353072e-5
allele num: 80924
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1868-26T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.313T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1853-26T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1907-26T>C
  variant of: http://identifiers.org/hgnc/2555
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5314
  bin: 7.5e0
  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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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 6.75e1
  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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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
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
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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
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 888
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

X-119672093-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672093
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672093
    reference: chr 0
allele count: 76
allele frequency: 9.424720048611714e-4
allele num: 80639
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1907-29T>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1853-29T>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.310T>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1868-29T>A
  variant of: http://identifiers.org/hgnc/2555
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12741
  bin: 2.75e1
  variant carriers: 7
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: 5
genotype depth: GenotypeDepth
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  variant carriers: 7
genotype depth: GenotypeDepth
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  variant carriers: 2
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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  variant carriers: 14
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1756
  bin: 7.75e1
  variant carriers: 2
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

X-119672101-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672101
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672101
    reference: chr 0
allele count: 248
allele frequency: 3.132855825469613e-3
allele num: 79161
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1907-37C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.302C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1853-37C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1868-37C>T
  variant of: http://identifiers.org/hgnc/2555
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15634
  bin: 1.25e1
  variant carriers: 16
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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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 2
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9601
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  variant carriers: 41
genotype depth: GenotypeDepth
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  variant carriers: 23
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
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  variant carriers: 10
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 31
genotype depth: GenotypeDepth
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  variant carriers: 4
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 225
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  variant carriers: 1
genotype quality: GenotypeQuality
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  variant carriers: 5
genotype quality: GenotypeQuality
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  variant carriers: 4
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 1
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 5
genotype quality: GenotypeQuality
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  bin: 2.75e1
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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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  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 604
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 4
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

X-119672103-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672103
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672103
    reference: chr 0
allele count: 3
allele frequency: 3.818785880675671e-5
allele num: 78559
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.300C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1868-39C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1853-39C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1907-39C>T
  variant of: http://identifiers.org/hgnc/2555
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

X-119672110-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672110
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672110
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 77269
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158290
  ensembl transcript: ENST00000497616
  gene symbol: CUL4B
  hgvsc: ENST00000497616.1:n.293T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1907-46T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1868-46T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1853-46T>C
  variant of: http://identifiers.org/hgnc/2555
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
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 depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

X-119672478-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672478
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672478
    reference: chr 0
allele count: 1
allele frequency: 1.147315282239559e-5
allele num: 87160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1867+37T>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1852+37T>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1906+37T>A
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
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site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
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site quality: ClippingRankSum

X-119672499-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672499
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672499
    reference: chr 0
allele count: 1
allele frequency: 1.144727955401399e-5
allele num: 87357
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1852+16T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1867+16T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1906+16T>C
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 471
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum

X-119672504-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672504
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672504
    reference: chr 0
allele count: 1
allele frequency: 1.144138578064575e-5
allele num: 87402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1852+11C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1867+11C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1906+11C>T
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 2407
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genotype depth: GenotypeDepth
  all individuals: 302
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 4
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

X-119672570-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672570
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672570
    reference: chr 0
allele count: 36
allele frequency: 4.114379757251594e-4
allele num: 87498
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1851C>T
  hgvsp: ENST00000404115.3:c.1851C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1797C>T
  hgvsp: ENST00000371322.5:c.1797C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1812C>T
  hgvsp: ENST00000336592.6:c.1812C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 3.25e1
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genotype depth: GenotypeDepth
  all individuals: 344
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  variant carriers: 2
genotype depth: GenotypeDepth
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  variant carriers: 4
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 5734
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  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 12
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  variant carriers: 0
hgvs: p.Val617Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

X-119672594-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672594
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672594
    reference: chr 0
allele count: 2
allele frequency: 2.29089826120822e-5
allele num: 87302
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1788A>G
  hgvsp: ENST00000336592.6:c.1788A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1827A>G
  hgvsp: ENST00000404115.3:c.1827A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1773A>G
  hgvsp: ENST00000371322.5:c.1773A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11589
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 2
genotype depth: GenotypeDepth
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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
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Lys609Lys
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

X-119672601-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672601
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672601
    reference: chr 0
allele count: 1
allele frequency: 1.146670641791558e-5
allele num: 87209
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1820A>T
  hgvsp: ENSP00000384109.3:p.Tyr607Phe
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1766A>T
  hgvsp: ENSP00000360373.5:p.Tyr589Phe
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1781A>T
  hgvsp: ENSP00000338919.6:p.Tyr594Phe
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Tyr607Phe
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

X-119672628-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672628
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672628
    reference: chr 0
allele count: 1
allele frequency: 1.169030055762734e-5
allele num: 85541
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1796-3T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1742-3T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1757-3T>C
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: splice region
filter: PASS
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 depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 153
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  variant carriers: 0
hgvs: c.1796-3T>C
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

X-119672630-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672630
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672630
    reference: chr 0
allele count: 2
allele frequency: 2.342523835180023e-5
allele num: 85378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1757-5C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1742-5C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1796-5C>T
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  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
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 8142
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  variant carriers: 0
hgvs: c.1796-5C>T
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

X-119672633-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672633
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672633
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 84915
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1757-8T>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1796-8T>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1742-8T>A
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 123
  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 depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: c.1796-8T>A
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-119672634-A-ATATG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672634
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672638
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 84333
alternate allele: ATATG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1742-10_1742-9insCATA
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1757-10_1757-9insCATA
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1796-10_1796-9insCATA
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 7900
  bin: 2.25e1
  variant carriers: 1
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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genotype quality: GenotypeQuality
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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: 478
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  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP

X-119672636-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672636
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672636
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 84344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1742-11T>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1757-11T>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1796-11T>A
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
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site quality: MQRankSum

X-119672641-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672641
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672641
    reference: chr 0
allele count: 2
allele frequency: 2.391114618079218e-5
allele num: 83643
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1757-16A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1742-16A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1796-16A>G
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

X-119672655-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672655
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672655
    reference: chr 0
allele count: 1
allele frequency: 1.22391530506089e-5
allele num: 81705
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1742-30A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1757-30A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1796-30A>G
  variant of: http://identifiers.org/hgnc/2555
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: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

X-119672662-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672662
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672662
    reference: chr 0
allele count: 2
allele frequency: 2.47939007004277e-5
allele num: 80665
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1757-37T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1796-37T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1742-37T>C
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
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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num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

X-119672673-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672673
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672673
    reference: chr 0
allele count: 1
allele frequency: 1.273155515946273e-5
allele num: 78545
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1757-48A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1796-48A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1742-48A>G
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  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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num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
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site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
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X-119672676-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119672676
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119672676
    reference: chr 0
allele count: 2
allele frequency: 2.55842810177427e-5
allele num: 78173
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1796-51G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1742-51G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1757-51G>A
  variant of: http://identifiers.org/hgnc/2555
canonical: true
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filter: PASS
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
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site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
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X-119673074-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119673074
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119673074
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 17006
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1741+49A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1756+49A>G
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
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  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1795+49A>G
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
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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: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD

X-119673083-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119673083
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119673083
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 17245
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1741+40T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1795+40T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1756+40T>C
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: AC_Adj0_Filter
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 (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: A
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

X-119673141-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119673141
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119673141
    reference: chr 0
allele count: 1
allele frequency: 2.510292198011849e-5
allele num: 39836
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1738A>G
  hgvsp: ENSP00000338919.6:p.Ile580Val
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1723A>G
  hgvsp: ENSP00000360373.5:p.Ile575Val
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
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  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1777A>G
  hgvsp: ENSP00000384109.3:p.Ile593Val
  variant of: http://identifiers.org/hgnc/2555
canonical: true
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  bin: 8.25e1
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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
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  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile593Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

X-119673142-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119673142
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119673142
    reference: chr 0
allele count: 1
allele frequency: 2.466395363176717e-5
allele num: 40545
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1737C>T
  hgvsp: ENST00000336592.6:c.1737C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1776C>T
  hgvsp: ENST00000404115.3:c.1776C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1722C>T
  hgvsp: ENST00000371322.5:c.1722C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: synonymous
filter: PASS
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
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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hgvs: p.Ile592Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

X-119673169-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119673169
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119673169
    reference: chr 0
allele count: 1
allele frequency: 1.807305127324646e-5
allele num: 55331
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1749T>G
  hgvsp: ENST00000404115.3:c.1749T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1710T>G
  hgvsp: ENST00000336592.6:c.1710T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1695T>G
  hgvsp: ENST00000371322.5:c.1695T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Leu583Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

X-119673214-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119673214
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119673214
    reference: chr 0
allele count: 1
allele frequency: 1.781927689374365e-5
allele num: 56119
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1665T>C
  hgvsp: ENST00000336592.6:c.1665T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1650T>C
  hgvsp: ENST00000371322.5:c.1650T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1704T>C
  hgvsp: ENST00000404115.3:c.1704T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
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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 quality: GenotypeQuality
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hgvs: p.Asp568Asp
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

X-119673237-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119673237
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119673237
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 49431
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1691-10C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1652-10C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1637-10C>T
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

X-119673239-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119673239
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119673239
    reference: chr 0
allele count: 1
allele frequency: 2.053008684226734e-5
allele num: 48709
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1691-12C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1652-12C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
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  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1637-12C>T
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
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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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: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
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site quality: MQ
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site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

X-119673240-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119673240
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119673240
    reference: chr 0
allele count: 3
allele frequency: 6.162695152013147e-5
allele num: 48680
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1637-13T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1652-13T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1691-13T>C
  variant of: http://identifiers.org/hgnc/2555
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: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
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X-119673248-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119673248
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119673248
    reference: chr 0
allele count: 1
allele frequency: 2.170327285354631e-5
allele num: 46076
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1652-21C>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1637-21C>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
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  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1691-21C>A
  variant of: http://identifiers.org/hgnc/2555
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: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
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site quality: InbreedingCoeff
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site quality: VQSLOD
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site quality: QD
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X-119673260-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119673260
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119673260
    reference: chr 0
allele count: 1
allele frequency: 2.445107340212235e-5
allele num: 40898
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1691-33G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1652-33G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
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  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1637-33G>A
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
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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: 138
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

X-119673265-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119673265
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119673265
    reference: chr 0
allele count: 19
allele frequency: 4.86169750006397e-4
allele num: 39081
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1691-38C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1652-38C>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1637-38C>T
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  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 depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
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genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

X-119673272-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119673272
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119673272
    reference: chr 0
allele count: 4
allele frequency: 1.082807720419047e-4
allele num: 36941
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1637-45G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1691-45G>A
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1652-45G>A
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3506
  bin: 2.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 4
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

X-119673274-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119673274
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119673274
    reference: chr 0
allele count: 3
allele frequency: 8.230678482262888e-5
allele num: 36449
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1637-47T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1652-47T>C
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1691-47T>C
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 523
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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: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

X-119673279-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119673279
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119673279
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 35343
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1691-52G>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1652-52G>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1637-52G>T
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 202
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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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num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

X-119674179-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119674179
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119674179
    reference: chr 0
allele count: 1
allele frequency: 1.215465584091986e-5
allele num: 82273
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1651+46A>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1690+46A>T
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1636+46A>T
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8384
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14275
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2091
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2314
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1401
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4348
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1356
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4433
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4398
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2562
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3575
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5000
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23213
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

X-119674186-ACAT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24119674186
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24119674183
    reference: chr 0
allele count: 2
allele frequency: 2.423831107448433e-5
allele num: 82514
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000360373
  ensembl transcript: ENST00000371322
  gene symbol: CUL4B
  hgvsc: ENST00000371322.5:c.1636+36_1636+38delATG
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000338919
  ensembl transcript: ENST00000336592
  gene symbol: CUL4B
  hgvsc: ENST00000336592.6:c.1651+36_1651+38delATG
  variant of: http://identifiers.org/hgnc/2555
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158290
  ensembl protein: ENSP00000384109
  ensembl transcript: ENST00000404115
  gene symbol: CUL4B
  hgvsc: ENST00000404115.3:c.1690+36_1690+38delATG
  variant of: http://identifiers.org/hgnc/2555
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 4580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9641
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17631
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: ACAT

GenotypeQuality
all individuals: 1388
bin: 8.75e1
variant carriers: 22

GenotypeQuality
all individuals: 91
bin: 3.25e1
variant carriers: 17

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 11

GenotypeQuality
all individuals: 3592
bin: 7.75e1
variant carriers: 14

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10108
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 88
allele frequency: 2.190144350423096e-2
allele num: 4018
num of homozygotes: 0

East Asian
type: Population
allele count: 21
allele frequency: 3.211009174311927e-3
allele num: 6540
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 9.777294948397611e-4
allele num: 9205
num of homozygotes: 0

African
type: Population
allele count: 109
allele frequency: 1.415952195375422e-2
allele num: 7698
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 1.038062283737024e-2
allele num: 578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 379
allele frequency: 8.321805765979405e-3
allele num: 45543
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.197e1

MQ
type: SiteQuality
SIO_000300: 5.872e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.57e0

DP
type: SiteQuality
SIO_000300: 2.874844e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.988e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.441e0

FS
type: SiteQuality
SIO_000300: 2.73873e2

MQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

QD
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

GenotypeQuality
all individuals: 2361
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7336
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2398
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9205
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7698
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4018
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.195727115034143e-5
allele num: 45543
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10108
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.441e0

VQSLOD
type: SiteQuality
SIO_000300: -8.197e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.988e0

MQ
type: SiteQuality
SIO_000300: 5.872e1

FS
type: SiteQuality
SIO_000300: 2.73873e2

QD
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

DP
type: SiteQuality
SIO_000300: 2.874844e6

GenotypeQuality
all individuals: 18679
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7310
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10082
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
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: 2
allele frequency: 2.3767082590612e-4
allele num: 8415
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9292
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.481718e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.550000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e0

VQSLOD
type: SiteQuality
SIO_000300: 2.44e-1

QD
type: SiteQuality
SIO_000300: 1.672e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.914e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.92e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 2326
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.209817293929443e-5
allele num: 47508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10073
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8355
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: 9.1e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.109e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.67e-2

FS
type: SiteQuality
SIO_000300: 2.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.15e-1

DP
type: SiteQuality
SIO_000300: 2.42393e6

VQSLOD
type: SiteQuality
SIO_000300: -1.377e0

MQ
type: SiteQuality
SIO_000300: 5.83e1

QD
type: SiteQuality
SIO_000300: 1.641e1

GenotypeQuality
all individuals: 216
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8286
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10076
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.224489364848024e-5
allele num: 47343
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.3e-1

MQ
type: SiteQuality
SIO_000300: 5.889e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.071e0

VQSLOD
type: SiteQuality
SIO_000300: -2.283e0

DP
type: SiteQuality
SIO_000300: 2.403473e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.83e0

GenotypeQuality
all individuals: 1167
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6484
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2862
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47408
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.926543577526305e-5
allele num: 10074
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6511
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.385804e6

QD
type: SiteQuality
SIO_000300: 3.212e1

GenotypeQuality
all individuals: 111
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1363
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8311
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9247
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10068
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.113182029500021e-5
allele num: 47322
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.361382e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.224e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

MQRankSum
type: SiteQuality
SIO_000300: -4.716e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.76e-1

QD
type: SiteQuality
SIO_000300: 5.54e0

MQ
type: SiteQuality
SIO_000300: 5.198e1

GenotypeQuality
all individuals: 75
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1800
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 8.553771143853046e-5
allele num: 46763
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9170
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6515
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: 9892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4472
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.974e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

FS
type: SiteQuality
SIO_000300: 2.608e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.96e0

MQRankSum
type: SiteQuality
SIO_000300: -6.3e-2

DP
type: SiteQuality
SIO_000300: 1.779732e6

QD
type: SiteQuality
SIO_000300: 1.029e1

GenotypeQuality
all individuals: 8555
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2219
bin: 7.25e1
variant carriers: 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: 46788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4479
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9173
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.947424765076722e-4
allele num: 8407
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.5e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

FS
type: SiteQuality
SIO_000300: 9.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.571e0

DP
type: SiteQuality
SIO_000300: 1.795633e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.35e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.25e-1

GenotypeQuality
all individuals: 6374
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1110
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46934
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8413
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.528117359413203e-4
allele num: 6544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4483
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9183
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.055e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.53e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 8.21e-1

DP
type: SiteQuality
SIO_000300: 1.808967e6

QD
type: SiteQuality
SIO_000300: 2.656e1

GenotypeQuality
all individuals: 2419
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28604
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46934
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.188636633781053e-4
allele num: 8413
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9183
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: 4483
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.21e-1

DP
type: SiteQuality
SIO_000300: 1.808967e6

QD
type: SiteQuality
SIO_000300: 2.656e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.055e0

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.53e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e0

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2236
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8560
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.116939751894661e-5
allele num: 47238
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6577
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8429
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9226
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4485
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9945
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.679999999999999e-1

FS
type: SiteQuality
SIO_000300: 8.102e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.069e0

QD
type: SiteQuality
SIO_000300: 1.205e1

VQSLOD
type: SiteQuality
SIO_000300: 2.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

DP
type: SiteQuality
SIO_000300: 1.83567e6

MQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47700
num of homozygotes: 0

South Asian
type: Population
allele count: 25
allele frequency: 2.493268175925002e-3
allele num: 10027
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
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: 1
allele frequency: 1.594896331738437e-3
allele num: 627
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4503
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.253e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-1

DP
type: SiteQuality
SIO_000300: 1.863713e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.63e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.544e0

QD
type: SiteQuality
SIO_000300: 2.169e1

MQRankSum
type: SiteQuality
SIO_000300: 3.03e-1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 3073
bin: 7.75e1
variant carriers: 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: 630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9288
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.511030522816561e-4
allele num: 6618
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47823
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10064
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

QD
type: SiteQuality
SIO_000300: 1.878e1

MQRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.177e0

DP
type: SiteQuality
SIO_000300: 1.86989e6

FS
type: SiteQuality
SIO_000300: 5.972e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2426
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 2.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.510345869204048e-4
allele num: 6621
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47856
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9292
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10078
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.978e1

QD
type: SiteQuality
SIO_000300: 1.197e1

FS
type: SiteQuality
SIO_000300: 6.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.981e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.27e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 1.872433e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.02e-1

GenotypeQuality
all individuals: 3076
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1797
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8561
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10099
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9303
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4520
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: 8497
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47918
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0142e1

MQ
type: SiteQuality
SIO_000300: 5.976e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.92e-1

QD
type: SiteQuality
SIO_000300: 1.284e1

VQSLOD
type: SiteQuality
SIO_000300: -5.359e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.19e-1

DP
type: SiteQuality
SIO_000300: 1.875333e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47933
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: 8499
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 4.297378599054577e-4
allele num: 9308
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.529e-1

DP
type: SiteQuality
SIO_000300: 1.876267e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.98e-1

FS
type: SiteQuality
SIO_000300: 4.968e0

VQSLOD
type: SiteQuality
SIO_000300: 4.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.46e0

QD
type: SiteQuality
SIO_000300: 2.023e1

MQ
type: SiteQuality
SIO_000300: 5.977e1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.170315692897953e-5
allele num: 47958
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8501
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.242e0

DP
type: SiteQuality
SIO_000300: 1.877558e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.674e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-1

QD
type: SiteQuality
SIO_000300: 2.919e1

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 331
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.879345987596316e-4
allele num: 47889
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10100
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6622
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -2.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.673e-1

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.387e1

DP
type: SiteQuality
SIO_000300: 1.875643e6

FS
type: SiteQuality
SIO_000300: 1.89e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 94
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47532
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.160527168629145e-4
allele num: 9257
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8437
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4499
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6599
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.75e-2

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.849781e6

QD
type: SiteQuality
SIO_000300: 2.225e1

FS
type: SiteQuality
SIO_000300: 9.156000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.917e1

MQRankSum
type: SiteQuality
SIO_000300: -2.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.235e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2398
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4495
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9241
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10009
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8421
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.110550642662671e-5
allele num: 47381
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.971e1

MQRankSum
type: SiteQuality
SIO_000300: 4.35e-1

DP
type: SiteQuality
SIO_000300: 1.834272e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.256e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.97e-1

QD
type: SiteQuality
SIO_000300: 1.601e1

GenotypeQuality
all individuals: 285
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2381
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9205
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9978
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8405
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: 4484
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6551
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 3.182956329839155e-4
allele num: 47126
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.226e-1

DP
type: SiteQuality
SIO_000300: 1.793665e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: 2.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.79e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.01e-1

QD
type: SiteQuality
SIO_000300: 2.403e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.78e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9192
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: 4481
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.192037191560377e-4
allele num: 8389
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9957
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6541
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46979
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.84e1

VQSLOD
type: SiteQuality
SIO_000300: 5.610000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.49e-1

QD
type: SiteQuality
SIO_000300: 1.359e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.88e0

DP
type: SiteQuality
SIO_000300: 1.764693e6

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
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variant carriers: 0

GenotypeQuality
all individuals: 1089
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6365
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9031
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8215
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9775
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4431
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.18842324105482e-5
allele num: 45695
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 603
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.15e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.308e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.11e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.672e-1

QD
type: SiteQuality
SIO_000300: 8.710000000000001e0

DP
type: SiteQuality
SIO_000300: 1.651546e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.09e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6327
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45513
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.440214738897023e-4
allele num: 8196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 603
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9018
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.644e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQRankSum
type: SiteQuality
SIO_000300: 1.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.02e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.64e0

DP
type: SiteQuality
SIO_000300: 1.646089e6

GenotypeQuality
all individuals: 2752
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1704
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2590
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 597
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8991
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.027221366204417e-4
allele num: 9735
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8165
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4413
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6313
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.644864e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.14e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.996e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 658
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5220
bin: 9.75e1
variant carriers: 5

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.119137934688169e-5
allele num: 47189
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9683
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4499
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.967299200381908e-4
allele num: 8379
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9204
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.388e0

VQSLOD
type: SiteQuality
SIO_000300: -4.374e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 8.612e0

MQRankSum
type: SiteQuality
SIO_000300: 5.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.44e-2

DP
type: SiteQuality
SIO_000300: 1.685864e6

QD
type: SiteQuality
SIO_000300: 1.98e1

GenotypeQuality
all individuals: 28014
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1804
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8386
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9207
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4503
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47230
num of homozygotes: 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: 6595
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.031246777353821e-4
allele num: 9697
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.687052e6

MQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

QD
type: SiteQuality
SIO_000300: 2.209e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.46e0

VQSLOD
type: SiteQuality
SIO_000300: -1.167e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.384358607534573e-4
allele num: 8388
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6591
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4500
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.618122977346278e-3
allele num: 618
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: 9699
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47255
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.18e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.70986e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.13e0

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

VQSLOD
type: SiteQuality
SIO_000300: -1.181e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

QD
type: SiteQuality
SIO_000300: 2.251e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1430
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47435
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9807
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4508
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 1.081548777849881e-4
allele num: 9246
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.158e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e0

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.88e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.52e-1

QD
type: SiteQuality
SIO_000300: 1.161e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40341
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10003
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4514
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: 6629
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9284
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African
type: Population
allele count: 1
allele frequency: 1.183572020357439e-4
allele num: 8449
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47740
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

QD
type: SiteQuality
SIO_000300: 1.126e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e0

FS
type: SiteQuality
SIO_000300: 3.589e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e0

DP
type: SiteQuality
SIO_000300: 1.788341e6

VQSLOD
type: SiteQuality
SIO_000300: -6.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.12e-2

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47750
num of homozygotes: 0

European (Finnish)
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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: 9286
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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allele num: 10004
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Other
type: Population
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allele frequency: 0.0e0
allele num: 625
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6629
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.822e0

FS
type: SiteQuality
SIO_000300: 1.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.148e0

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 9.599999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e0

DP
type: SiteQuality
SIO_000300: 1.789426e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 913
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9281
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.001000500250125e-4
allele num: 9995
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African
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allele count: 1
allele frequency: 1.183852255238546e-4
allele num: 8447
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: 47736
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-1

DP
type: SiteQuality
SIO_000300: 1.790112e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.649999999999999e-1

FS
type: SiteQuality
SIO_000300: 8.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.766e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.271e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.91e-2

QD
type: SiteQuality
SIO_000300: 6.66e0

GenotypeQuality
all individuals: 6921
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2075
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 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: 8400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.109793662179839e-5
allele num: 47398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4501
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9226
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9853
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.86e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.59e-2

MQ
type: SiteQuality
SIO_000300: 5.687e1

QD
type: SiteQuality
SIO_000300: 3.091e1

DP
type: SiteQuality
SIO_000300: 1.773788e6

GenotypeQuality
all individuals: 632
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6657
bin: 6.75e1
variant carriers: 10

GenotypeQuality
all individuals: 1686
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 564
bin: 3.25e1
variant carriers: 2

Other
type: Population
allele count: 1
allele frequency: 1.628664495114007e-3
allele num: 614
num of homozygotes: 0

South Asian
type: Population
allele count: 47
allele frequency: 4.899405816741374e-3
allele num: 9593
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 125
allele frequency: 2.677634256581625e-3
allele num: 46683
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.202067556196658e-4
allele num: 8319
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 5.458515283842794e-4
allele num: 9160
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.793e1

FS
type: SiteQuality
SIO_000300: 6.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-1

DP
type: SiteQuality
SIO_000300: 1.735698e6

VQSLOD
type: SiteQuality
SIO_000300: 2.406e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.467e0

GenotypeQuality
all individuals: 622
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1833
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23878
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4383
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.746721618583739e-4
allele num: 8007
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6316
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.694934166480696e-5
allele num: 44810
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.409999999999999e-1

QD
type: SiteQuality
SIO_000300: 9.449999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: -1.94e-1

DP
type: SiteQuality
SIO_000300: 1.554809e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.37e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

MQ
type: SiteQuality
SIO_000300: 5.777e1

GenotypeQuality
all individuals: 1310
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1817
bin: 7.75e1
variant carriers: 1

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

African
type: Population
allele count: 2
allele frequency: 2.512562814070352e-4
allele num: 7960
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6274
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4373
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44587
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8951
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.83e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

DP
type: SiteQuality
SIO_000300: 1.525621e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 887
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4562
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8822
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.530364372469636e-4
allele num: 7904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44226
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8867
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6236
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 582
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4363
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

QD
type: SiteQuality
SIO_000300: 2.564e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.45e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.547e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.66e0

MQRankSum
type: SiteQuality
SIO_000300: -3.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.076e0

DP
type: SiteQuality
SIO_000300: 1.481645e6

GenotypeQuality
all individuals: 617
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5137
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 492
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4363
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6226
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44177
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8847
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.792667509481669e-4
allele num: 7910
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 581
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.61e-1

QD
type: SiteQuality
SIO_000300: 1.963e1

FS
type: SiteQuality
SIO_000300: 2.411e0

MQRankSum
type: SiteQuality
SIO_000300: 6.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

DP
type: SiteQuality
SIO_000300: 1.47243e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 5167
bin: 9.75e1
variant carriers: 61

GenotypeQuality
all individuals: 4923
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 5.75e1
variant carriers: 1

Latino
type: Population
allele count: 3
allele frequency: 3.40522133938706e-4
allele num: 8810
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.273192243868064e-5
allele num: 43991
num of homozygotes: 0

African
type: Population
allele count: 72
allele frequency: 9.119696010132995e-3
allele num: 7895
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4358
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6203
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.451534e6

FS
type: SiteQuality
SIO_000300: 1.163e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.45e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

QD
type: SiteQuality
SIO_000300: 1.808e1

VQSLOD
type: SiteQuality
SIO_000300: 2.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

GenotypeQuality
all individuals: 11954
bin: 6.25e1
variant carriers: 7

GenotypeQuality
all individuals: 1473
bin: 4.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1680
bin: 7.75e1
variant carriers: 1

East Asian
type: Population
allele count: 51
allele frequency: 8.389537752919889e-3
allele num: 6079
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 2.548656163113994e-4
allele num: 43160
num of homozygotes: 0

Latino
type: Population
allele count: 183
allele frequency: 2.110483219928497e-2
allele num: 8671
num of homozygotes: 4

African
type: Population
allele count: 1
allele frequency: 1.284191601386927e-4
allele num: 7787
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4319
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.745200698080279e-3
allele num: 573
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.166588894073728e-4
allele num: 8572
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.636e1

MQRankSum
type: SiteQuality
SIO_000300: 2.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.262e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.037e0

VQSLOD
type: SiteQuality
SIO_000300: 5.57e0

DP
type: SiteQuality
SIO_000300: 1.374458e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1833
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5097
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 6425
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6022
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.473026163463765e-4
allele num: 8638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7733
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4299
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42801
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e-2

QD
type: SiteQuality
SIO_000300: 1.304e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.18e0

FS
type: SiteQuality
SIO_000300: 4.595e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.01e-1

DP
type: SiteQuality
SIO_000300: 1.357255e6

GenotypeQuality
all individuals: 5095
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1248
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1624
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5930
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42027
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8303
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7644
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 559
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8533
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4273
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.34e-1

QD
type: SiteQuality
SIO_000300: 7.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.669e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e0

VQSLOD
type: SiteQuality
SIO_000300: -1.024e0

DP
type: SiteQuality
SIO_000300: 1.322742e6

GenotypeQuality
all individuals: 903
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6555
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8429
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.916699722332408e-5
allele num: 10084
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.52e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.158e0

DP
type: SiteQuality
SIO_000300: 1.84405e6

QD
type: SiteQuality
SIO_000300: 1.296e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.331e0

VQSLOD
type: SiteQuality
SIO_000300: 3.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.64e-1

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10103
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.092312842616228e-5
allele num: 47794
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.055e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

DP
type: SiteQuality
SIO_000300: 1.857745e6

QD
type: SiteQuality
SIO_000300: 1.667e1

VQSLOD
type: SiteQuality
SIO_000300: -3.915e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.554e0

MQRankSum
type: SiteQuality
SIO_000300: 8.2e-1

GenotypeQuality
all individuals: 1328
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
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: 2.09148139627298e-5
allele num: 47813
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6589
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Other
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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MQRankSum
type: SiteQuality
SIO_000300: 5.629999999999999e-1

ClippingRankSum
type: SiteQuality
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MQ
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QD
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.49e-1

GenotypeQuality
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bin: 8.75e1
variant carriers: 1

South Asian
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allele frequency: 3.364005144949045e-3
allele num: 10107
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4523
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East Asian
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allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 630
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African
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allele frequency: 1.187648456057007e-4
allele num: 8420
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 9304
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.0875083500334e-5
allele num: 47904
num of homozygotes: 0

MQ
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.78e-1

FS
type: SiteQuality
SIO_000300: 2.491e0

VQSLOD
type: SiteQuality
SIO_000300: 1.788e1

DP
type: SiteQuality
SIO_000300: 1.865007e6

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 8309
num of homozygotes: 0

East Asian
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allele frequency: 3.027092477675193e-4
allele num: 6607
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South Asian
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allele frequency: 0.0e0
allele num: 10105
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47847
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Other
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allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9283
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European (Finnish)
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allele frequency: 0.0e0
allele num: 4520
num of homozygotes: 0

DP
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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FS
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QD
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VQSLOD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.55e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
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allele frequency: 0.0e0
allele num: 10101
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 2.092006443379846e-5
allele num: 47801
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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QD
type: SiteQuality
SIO_000300: 1.324e1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
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SIO_000300: 5.969e1

ClippingRankSum
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ReadPosRankSum
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.66e0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.85671e6

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

East Asian
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allele frequency: 1.545356204605162e-4
allele num: 6471
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4483
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9182
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South Asian
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allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 620
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 7897
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 46887
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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SIO_000300: -7.19e-1

MQ
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SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 2.016e1

DP
type: SiteQuality
SIO_000300: 1.804484e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.58e0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9171
num of homozygotes: 0

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

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

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

African
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allele count: 2
allele frequency: 2.540327702273593e-4
allele num: 7873
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 46788
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4477
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.288e0

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.88e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.95e-1

DP
type: SiteQuality
SIO_000300: 1.797909e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6431
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9946
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 46499
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 618
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.204e0

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 3.973e1

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.774414e6

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9121
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7756
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 46098
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 6380
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 615
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4449
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 9914
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.559e0

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.804e0

DP
type: SiteQuality
SIO_000300: 1.742831e6

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9120
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4447
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7767
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 46101
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 615
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9871
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9076
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 6293
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 4.376750700280112e-5
allele num: 45696
num of homozygotes: 0

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
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MQ
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
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allele frequency: 0.0e0
allele num: 6101
num of homozygotes: 0

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

Latino
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allele frequency: 1.11731843575419e-4
allele num: 8950
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 4373
num of homozygotes: 0

DP
type: SiteQuality
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FS
type: SiteQuality
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MQ
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele frequency: 4.566835639585331e-5
allele num: 43794
num of homozygotes: 0

ReadPosRankSum
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MQ
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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QD
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ClippingRankSum
type: SiteQuality
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
type: SiteQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
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allele frequency: 1.055631795629684e-4
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Other
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East Asian
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allele frequency: 0.0e0
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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ReadPosRankSum
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VQSLOD
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FS
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QD
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MQ
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MQRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
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num of homozygotes: 0

East Asian
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European (Finnish)
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.371241582092384e-5
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num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 8998
num of homozygotes: 0

InbreedingCoeff
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FS
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VQSLOD
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DP
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MQ
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QD
type: SiteQuality
SIO_000300: 2.328e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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

QD
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MQ
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DP
type: SiteQuality
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FS
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VQSLOD
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

Other
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 5.132152938157557e-5
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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QD
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FS
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ReadPosRankSum
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MQ
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DP
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 4388
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African
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East Asian
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Other
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 5.051525560719337e-5
allele num: 19796
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 2780
num of homozygotes: 0

East Asian
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Other
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South Asian
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European (Non-Finnish)
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allele frequency: 3.613761202659729e-5
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African
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allele frequency: 0.0e0
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Latino
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InbreedingCoeff
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FS
type: SiteQuality
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DP
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MQRankSum
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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QD
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MQ
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ClippingRankSum
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GenotypeQuality
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variant carriers: 1

South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 1.406271972999578e-4
allele num: 7111
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

African
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Other
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South Asian
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European (Finnish)
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Latino
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allele frequency: 1.979414093428345e-4
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European (Non-Finnish)
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East Asian
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MQRankSum
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FS
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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MQ
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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QD
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DP
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GenotypeQuality
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bin: 5.75e1
variant carriers: 1

Other
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allele frequency: 0.0e0
allele num: 390
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.241516305247476e-4
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Latino
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African
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East Asian
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DP
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InbreedingCoeff
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VQSLOD
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MQ
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QD
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ClippingRankSum
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FS
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 4696
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 4.408004936965529e-5
allele num: 22686
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Other
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African
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East Asian
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European (Finnish)
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South Asian
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FS
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MQ
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ClippingRankSum
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QD
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DP
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele frequency: 5.043373007867662e-5
allele num: 19828
num of homozygotes: 0

African
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South Asian
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East Asian
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Latino
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European (Finnish)
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Other
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FS
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InbreedingCoeff
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DP
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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QD
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
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allele frequency: 8.475474096832291e-4
allele num: 18878
num of homozygotes: 0

Latino
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East Asian
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Other
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African
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South Asian
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European (Finnish)
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allele frequency: 1.378043178686265e-3
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num of homozygotes: 0

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

European (Non-Finnish)
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South Asian
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African
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Other
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Latino
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European (Finnish)
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East Asian
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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VQSLOD
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DP
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MQRankSum
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InbreedingCoeff
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MQ
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QD
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 2501
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2057
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17068
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5482
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3007
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4906
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.84327e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.29e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.5e0

VQSLOD
type: SiteQuality
SIO_000300: -1.175e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

QD
type: SiteQuality
SIO_000300: 1.334e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.22e-1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44443
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8233
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8887
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 597
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.052299273913501e-4
allele num: 9503
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6201
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4409
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.55e-1

QD
type: SiteQuality
SIO_000300: 3.01e1

VQSLOD
type: SiteQuality
SIO_000300: -3.011e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.74e-1

DP
type: SiteQuality
SIO_000300: 1.355916e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.48e-1