1-66723580-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66723580
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66723580
    reference: chr 1
allele count: 1
allele frequency: 8.422187410514259e-6
allele num: 118734
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.584+34C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.108+34C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.539+34C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.248+34C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.210+34C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.584+34C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.308+34C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.584+34C>T
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3500
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
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genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
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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  bin: 4.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
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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: 8.25e1
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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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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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3057
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

1-66723590-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66723590
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66723590
    reference: chr 1
allele count: 1
allele frequency: 8.479031355457952e-6
allele num: 117938
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.248+44G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.210+44G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.584+44G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.308+44G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.539+44G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.584+44G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.108+44G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.584+44G>A
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 125
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genotype depth: GenotypeDepth
  all individuals: 216
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7100
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 77
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

1-66731670-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731670
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731670
    reference: chr 1
allele count: 2
allele frequency: 1.659585767392459e-5
allele num: 120512
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.249-51A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.309-51A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.585-51A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.109-51A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.585-51A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.585-51A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.211-51A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.540-51A>T
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1466
  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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 528
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

1-66731680-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731680
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731680
    reference: chr 1
allele count: 2
allele frequency: 1.657330372236402e-5
allele num: 120676
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.249-41T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.211-41T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.585-41T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.585-41T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.540-41T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.109-41T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.585-41T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.309-41T>C
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  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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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1085
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3949
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

1-66731681-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731681
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731681
    reference: chr 1
allele count: 1
allele frequency: 8.286514526259965e-6
allele num: 120678
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.585-40T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.211-40T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.309-40T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.109-40T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.585-40T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.540-40T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.585-40T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.249-40T>G
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1087
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41076
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1631
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

1-66731690-GACTCAGTCCTTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731690
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731678
    reference: chr 1
allele count: 1
allele frequency: 8.284180528862085e-6
allele num: 120712
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1045
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1362
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3941
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: GACTCAGTCCTTC
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

1-66731691-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731691
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731691
    reference: chr 1
allele count: 34
allele frequency: 2.816248094890995e-4
allele num: 120728
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.540-30A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.249-30A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.211-30A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.585-30A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.585-30A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.585-30A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.309-30A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.109-30A>G
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25951
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17742
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8380
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1365
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1059
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 1
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-66731696-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731696
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731696
    reference: chr 1
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.585-25G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.309-25G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.249-25G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.585-25G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.585-25G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.540-25G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.211-25G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.109-25G>A
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1036
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

1-66731705-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731705
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731705
    reference: chr 1
allele count: 1
allele frequency: 8.275268532463878e-6
allele num: 120842
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.585-16T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.540-16T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.309-16T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.249-16T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.211-16T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.109-16T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.585-16T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.585-16T>G
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8409
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
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genotype depth: GenotypeDepth
  all individuals: 26481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
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genotype depth: GenotypeDepth
  all individuals: 255
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.75e1
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genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
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genotype depth: GenotypeDepth
  all individuals: 20
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genotype depth: GenotypeDepth
  all individuals: 82
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genotype depth: GenotypeDepth
  all individuals: 90
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genotype depth: GenotypeDepth
  all individuals: 191
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genotype depth: GenotypeDepth
  all individuals: 482
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 2177
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genotype depth: GenotypeDepth
  all individuals: 199
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genotype depth: GenotypeDepth
  all individuals: 385
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genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
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genotype quality: GenotypeQuality
  all individuals: 343
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 101
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genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 1341
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genotype quality: GenotypeQuality
  all individuals: 70
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 21
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genotype quality: GenotypeQuality
  all individuals: 739
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

1-66731709-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731709
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731709
    reference: chr 1
allele count: 1
allele frequency: 8.273762245168123e-6
allele num: 120864
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.109-12C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.249-12C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.585-12C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.540-12C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.585-12C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.585-12C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.211-12C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.309-12C>T
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18236
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8431
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
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genotype depth: GenotypeDepth
  all individuals: 26598
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genotype depth: GenotypeDepth
  all individuals: 2185
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
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genotype depth: GenotypeDepth
  all individuals: 268
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genotype depth: GenotypeDepth
  all individuals: 414
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genotype depth: GenotypeDepth
  all individuals: 770
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 136
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genotype depth: GenotypeDepth
  all individuals: 191
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 86
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genotype quality: GenotypeQuality
  all individuals: 44345
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum

1-66731714-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731714
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731714
    reference: chr 1
allele count: 1
allele frequency: 8.271024945411235e-6
allele num: 120904
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.540-7T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.309-7T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.585-7T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.109-7T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.211-7T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.585-7T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.585-7T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.249-7T>C
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 357
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genotype depth: GenotypeDepth
  all individuals: 230
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 77
  bin: 4.75e1
  variant carriers: 0
hgvs: c.585-7T>C
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum

1-66731715-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731715
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731715
    reference: chr 1
allele count: 1
allele frequency: 8.27034090345204e-6
allele num: 120914
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.309-6C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.109-6C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.585-6C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.585-6C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.540-6C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.249-6C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.585-6C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.211-6C>G
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44565
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
hgvs: c.585-6C>G
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

1-66731718-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731718
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731718
    reference: chr 1
allele count: 1
allele frequency: 8.268152729317216e-6
allele num: 120946
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.109-3C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.585-3C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.309-3C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.249-3C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.540-3C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.585-3C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.211-3C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.585-3C>T
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1533
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6129
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.25e1
  variant carriers: 0
hgvs: c.585-3C>T
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

1-66731723-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731723
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731723
    reference: chr 1
allele count: 1
allele frequency: 8.264736024331383e-6
allele num: 120996
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.311G>A
  hgvsp: ENSP00000397548.2:p.Arg104Lys
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.587G>A
  hgvsp: ENSP00000342637.4:p.Arg196Lys
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.587G>A
  hgvsp: ENSP00000332116.4:p.Arg196Lys
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.251G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.587G>A
  hgvsp: ENSP00000360088.3:p.Arg196Lys
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.111G>A
  hgvsp: ENSP00000432400.1:p.Arg38Lys
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.542G>A
  hgvsp: ENSP00000392947.2:p.Arg181Lys
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.213G>A
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg196Lys
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

1-66731724-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731724
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731724
    reference: chr 1
allele count: 2
allele frequency: 1.653001851362074e-5
allele num: 120992
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.588G>C
  hgvsp: ENSP00000332116.4:p.Arg196Ser
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.214G>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.252G>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.312G>C
  hgvsp: ENSP00000397548.2:p.Arg104Ser
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.112G>C
  hgvsp: ENSP00000432400.1:p.Arg38Ser
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.588G>C
  hgvsp: ENSP00000342637.4:p.Arg196Ser
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.543G>C
  hgvsp: ENSP00000392947.2:p.Arg181Ser
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.588G>C
  hgvsp: ENSP00000360088.3:p.Arg196Ser
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3930
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44862
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1342
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg196Ser
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

1-66731734-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731734
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731734
    reference: chr 1
allele count: 1
allele frequency: 8.261731658955718e-6
allele num: 121040
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.322G>A
  hgvsp: ENSP00000397548.2:p.Ala108Thr
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.598G>A
  hgvsp: ENSP00000360088.3:p.Ala200Thr
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.122G>A
  hgvsp: ENSP00000432400.1:p.Ala42Thr
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.224G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.598G>A
  hgvsp: ENSP00000342637.4:p.Ala200Thr
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.598G>A
  hgvsp: ENSP00000332116.4:p.Ala200Thr
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.553G>A
  hgvsp: ENSP00000392947.2:p.Ala185Thr
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.262G>A
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1344
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala200Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

1-66731735-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731735
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731735
    reference: chr 1
allele count: 1
allele frequency: 8.261458643138033e-6
allele num: 121044
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.554C>T
  hgvsp: ENSP00000392947.2:p.Ala185Val
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.263C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.599C>T
  hgvsp: ENSP00000342637.4:p.Ala200Val
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.123C>T
  hgvsp: ENSP00000432400.1:p.Ala42Val
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.225C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.599C>T
  hgvsp: ENSP00000360088.3:p.Ala200Val
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.599C>T
  hgvsp: ENSP00000332116.4:p.Ala200Val
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.323C>T
  hgvsp: ENSP00000397548.2:p.Ala108Val
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3928
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala200Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

1-66731741-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731741
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731741
    reference: chr 1
allele count: 1
allele frequency: 8.260230295220631e-6
allele num: 121062
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.605A>G
  hgvsp: ENSP00000342637.4:p.Gln202Arg
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.329A>G
  hgvsp: ENSP00000397548.2:p.Gln110Arg
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.269A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.129A>G
  hgvsp: ENSP00000432400.1:p.Gln44Arg
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.560A>G
  hgvsp: ENSP00000392947.2:p.Gln187Arg
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.605A>G
  hgvsp: ENSP00000332116.4:p.Gln202Arg
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.605A>G
  hgvsp: ENSP00000360088.3:p.Gln202Arg
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.231A>G
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1025
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln202Arg
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

1-66731742-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731742
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731742
    reference: chr 1
allele count: 1
allele frequency: 8.260503229856763e-6
allele num: 121058
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.130G>T
  hgvsp: ENSP00000432400.1:p.Gln44His
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.606G>T
  hgvsp: ENSP00000342637.4:p.Gln202His
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.606G>T
  hgvsp: ENSP00000332116.4:p.Gln202His
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.606G>T
  hgvsp: ENSP00000360088.3:p.Gln202His
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.330G>T
  hgvsp: ENSP00000397548.2:p.Gln110His
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.232G>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.270G>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.561G>T
  hgvsp: ENSP00000392947.2:p.Gln187His
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27116
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3928
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45059
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6148
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln202His
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum

1-66731763-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731763
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731763
    reference: chr 1
allele count: 1
allele frequency: 8.266649031148734e-6
allele num: 120968
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.627C>T
  hgvsp: ENST00000341517.4:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.627C>T
  hgvsp: ENST00000371049.3:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.291C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.351C>T
  hgvsp: ENST00000412480.2:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.253C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.582C>T
  hgvsp: ENST00000423207.2:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.627C>T
  hgvsp: ENST00000329654.4:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.151C>T
  hgvsp: ENST00000491340.2:c.151C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45055
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asn209Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP

1-66731774-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731774
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731774
    reference: chr 1
allele count: 1
allele frequency: 8.281436332317477e-6
allele num: 120752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+4G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.298+4G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+4G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+4G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+4G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.162G>A
  hgvsp: ENSP00000432400.1:p.Arg55Lys
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+4G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.260+4G>A
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1500
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg55Lys
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

1-66731777-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731777
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731777
    reference: chr 1
allele count: 1
allele frequency: 8.293386853323161e-6
allele num: 120578
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.298+7C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.165C>G
  hgvsp: ENSP00000432400.1:p.Pro56Arg
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+7C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+7C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+7C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.260+7C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+7C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+7C>G
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1007
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1317
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro56Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

1-66731779-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731779
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731779
    reference: chr 1
allele count: 1
allele frequency: 8.305233958440609e-6
allele num: 120406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.260+9T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+9T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.298+9T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+9T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+9T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+9T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+9T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.167T>C
  hgvsp: ENSP00000432400.1:p.Cys57Arg
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6085
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44540
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Cys57Arg
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

1-66731783-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731783
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731783
    reference: chr 1
allele count: 1
allele frequency: 8.324038157390913e-6
allele num: 120134
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+13A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+13A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+13A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+13A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.298+13A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.171A>G
  hgvsp: ENSP00000432400.1:p.His58Arg
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+13A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.260+13A>G
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 8
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genotype quality: GenotypeQuality
  all individuals: 1485
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genotype quality: GenotypeQuality
  all individuals: 28
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3924
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6071
  bin: 6.75e1
  variant carriers: 0
hgvs: p.His58Arg
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD

1-66731808-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731808
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731808
    reference: chr 1
allele count: 2
allele frequency: 1.766378746930917e-5
allele num: 113226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+38A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.196A>G
  hgvsp: ENST00000491340.2:c.196A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+38A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.260+38A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+38A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.298+38A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+38A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+38A>G
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12377
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1009
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 459
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 947
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8389
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg66Arg
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-66731812-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731812
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731812
    reference: chr 1
allele count: 5
allele frequency: 4.496079418746853e-5
allele num: 111208
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.*1A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+42A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+42A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+42A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+42A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.298+42A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+42A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.260+42A>G
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21481
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6918
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10798
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

1-66731816-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731816
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731816
    reference: chr 1
allele count: 1
allele frequency: 9.142272037446746e-6
allele num: 109382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+46A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+46A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.298+46A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+46A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+46A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.260+46A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.*5A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+46A>T
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19672
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5773
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1957
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3915
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1249
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12989
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-66731822-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731822
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731822
    reference: chr 1
allele count: 4
allele frequency: 3.795138427674149e-5
allele num: 105398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+52A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.298+52A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+52A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+52A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.*11A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.260+52A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+52A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+52A>G
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7073
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1178
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3916
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-66731824-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731824
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731824
    reference: chr 1
allele count: 5
allele frequency: 4.771811952434578e-5
allele num: 104782
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+54G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.298+54G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.*13G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.260+54G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+54G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+54G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+54G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+54G>A
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4889
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7683
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17779
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6826
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3807
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3571
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18791
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

1-66731825-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731825
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731825
    reference: chr 1
allele count: 2
allele frequency: 1.919238446184554e-5
allele num: 104208
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000432400
  ensembl transcript: ENST00000491340
  gene symbol: PDE4B
  hgvsc: ENST00000491340.2:c.*14C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+55C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.298+55C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.260+55C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+55C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+55C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+55C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+55C>T
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18683
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7864
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12894
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 896
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4097
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3914
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3802
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-66731854-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66731854
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66731854
    reference: chr 1
allele count: 32
allele frequency: 3.649468546142968e-4
allele num: 87684
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+84A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+84A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+84A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+84A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.298+84A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+84A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.260+84A>G
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14151
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20581
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9736
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3181
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2511
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2129
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7822
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1686
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

1-66732307-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732307
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732307
    reference: chr 1
allele count: 1
allele frequency: 1.848633859577772e-5
allele num: 54094
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+537T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+537T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+537T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.261-48T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.299-48T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+537T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+537T>A
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6504
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5925
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16003
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23946
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15149
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1178
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4869
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1020
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3684
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1519
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1808
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7879
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum

1-66732311-G-GTTTTGTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732311
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732318
    reference: chr 1
allele count: 2
allele frequency: 3.687995574405311e-5
allele num: 54230
alternate allele: GTTTTGTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.299-32_299-26dupGTTTTTT
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.261-32_261-26dupGTTTTTT
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6284
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23929
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
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genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1813
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19130
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3311
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4941
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 4128
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 239
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 6495
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genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD

1-66732315-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732315
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732315
    reference: chr 1
allele count: 14
allele frequency: 2.518619796351599e-4
allele num: 55586
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+545T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.261-40T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+545T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+545T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+545T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+545T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.299-40T>C
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24114
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 65
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16226
  bin: 1.25e1
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genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4467
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genotype depth: GenotypeDepth
  all individuals: 4091
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genotype depth: GenotypeDepth
  all individuals: 125
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
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genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 43
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4103
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3848
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 182
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 803
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3517
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4871
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6587
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-66732317-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732317
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732317
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 55462
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+547T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+547T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+547T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.299-38T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+547T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+547T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.261-38T>G
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4743
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16135
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5447
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1181
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2564
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4668
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4530
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

1-66732329-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732329
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732329
    reference: chr 1
allele count: 2
allele frequency: 3.443289029681151e-5
allele num: 58084
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.299-26T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+559T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.261-26T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+559T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+559T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+559T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+559T>A
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  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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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.5e0
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 9689
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

1-66732330-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732330
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732330
    reference: chr 1
allele count: 6
allele frequency: 1.032595601142739e-4
allele num: 58106
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+560A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+560A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+560A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+560A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.299-25A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.261-25A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+560A>T
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 3.25e1
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD

1-66732331-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732331
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732331
    reference: chr 1
allele count: 4
allele frequency: 6.825705607317156e-5
allele num: 58602
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+561A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+561A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+561A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+561A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.261-24A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+561A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.299-24A>T
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  bin: 9.75e1
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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: 1.25e1
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genotype quality: GenotypeQuality
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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: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/1-66732340-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732340
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732340
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 63016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+570C>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.261-15C>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+570C>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+570C>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+570C>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.299-15C>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+570C>A
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9822
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24323
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3528
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1208
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum

1-66732343-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732343
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732343
    reference: chr 1
allele count: 1
allele frequency: 1.548754801139884e-5
allele num: 64568
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+573C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.299-12C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+573C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+573C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.261-12C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+573C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+573C>T
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23802
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9126
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 1.75e1
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genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 2.75e1
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genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
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genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3268
  bin: 3.25e1
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genotype quality: GenotypeQuality
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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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  bin: 3.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP

1-66732346-ATCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732346
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732343
    reference: chr 1
allele count: 2
allele frequency: 3.022517757291824e-5
allele num: 66170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.261-7_261-5delCTT
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.299-7_299-5delCTT
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+578_589+580delCTT
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+578_634+580delCTT
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+578_634+580delCTT
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+578_358+580delCTT
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+578_634+580delCTT
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8641
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 1.75e1
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genotype depth: GenotypeDepth
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  bin: 8.25e1
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genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  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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  bin: 7.5e0
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  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: 2.75e1
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genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 162
  bin: 9.25e1
  variant carriers: 0
hgvs: n.261-7_261-5delCTT
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: ATCT
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD

1-66732346-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732346
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732346
    reference: chr 1
allele count: 2
allele frequency: 3.022517757291824e-5
allele num: 66170
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.261-9A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+576A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+576A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.299-9A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+576A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+576A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+576A>G
  variant of: http://identifiers.org/hgnc/8781
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  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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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8641
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24322
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1466
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17359
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3092
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1237
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

1-66732353-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732353
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732352
    reference: chr 1
allele count: 1
allele frequency: 1.441046776378361e-5
allele num: 69394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.261delG
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+585delG
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+585delG
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+585delG
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.299delG
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+585delG
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+585delG
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21721
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20260
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2719
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2675
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23014
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1285
  bin: 7.5e0
  variant carriers: 0
hgvs: n.261delG
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: AG
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/1-66732358-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732358
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732358
    reference: chr 1
allele count: 1
allele frequency: 1.386885609674914e-5
allele num: 72104
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+588A>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.264A>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+588A>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+588A>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.302A>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+588A>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+588A>C
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
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genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1760
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1229
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2514
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 178
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 623
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genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1186
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-66732359-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732359
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732359
    reference: chr 1
allele count: 1
allele frequency: 1.380376566727403e-5
allele num: 72444
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.265G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+589G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+589G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+589G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.303G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+589G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+589G>A
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7050
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 68
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 101
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genotype quality: GenotypeQuality
  all individuals: 370
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 520
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 21833
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 174
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

1-66732361-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732361
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732361
    reference: chr 1
allele count: 4
allele frequency: 5.457025920873124e-5
allele num: 73300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+591G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.305G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+591G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+591G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.267G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+591G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+591G>A
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19939
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6977
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  variant carriers: 1
genotype depth: GenotypeDepth
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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
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genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1176
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21398
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21597
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2451
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

1-66732365-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732365
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732365
    reference: chr 1
allele count: 104
allele frequency: 1.391676702796735e-3
allele num: 74730
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+595C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+595C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+595C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.309C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.271C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+595C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+595C>T
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21912
  bin: 2.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19303
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6906
  bin: 1.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 1.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2440
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2369
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20811
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1821
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 7.25e1
  variant carriers: 2
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

1-66732367-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732367
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732367
    reference: chr 1
allele count: 1
allele frequency: 1.327985976468088e-5
allele num: 75302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+597A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+597A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+597A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.311A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.273A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+597A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+597A>G
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19072
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6967
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 1234
  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2390
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genotype quality: GenotypeQuality
  all individuals: 421
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genotype quality: GenotypeQuality
  all individuals: 20602
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/1-66732368-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732368
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732368
    reference: chr 1
allele count: 2
allele frequency: 2.651113467656416e-5
allele num: 75440
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.274C>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+598C>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+598C>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+598C>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+598C>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.312C>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+598C>A
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18966
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6946
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21004
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20526
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2501
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 2394
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1235
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

1-66732386-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732386
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732386
    reference: chr 1
allele count: 42465
allele frequency: 4.599163886843131e-1
allele num: 92332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+616G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.292G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+616G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+616G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.330G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+616G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+616G>A
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 189
genotype depth: GenotypeDepth
  all individuals: 9977
  bin: 1.75e1
  variant carriers: 8897
genotype depth: GenotypeDepth
  all individuals: 9496
  bin: 7.5e0
  variant carriers: 2122
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 3.75e1
  variant carriers: 1048
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 2.75e1
  variant carriers: 3523
genotype depth: GenotypeDepth
  all individuals: 10241
  bin: 1.25e1
  variant carriers: 6844
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 2.5e0
  variant carriers: 138
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 3.25e1
  variant carriers: 1772
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 4.75e1
  variant carriers: 696
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 169
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 289
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 336
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 149
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.25e1
  variant carriers: 823
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 113
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 608
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 434
genotype depth: GenotypeDepth
  all individuals: 13561
  bin: 2.25e1
  variant carriers: 6590
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 9.75e1
  variant carriers: 812
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 5.75e1
  variant carriers: 659
genotype quality: GenotypeQuality
  all individuals: 690
  bin: 1.75e1
  variant carriers: 348
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 8.25e1
  variant carriers: 585
genotype quality: GenotypeQuality
  all individuals: 9051
  bin: 2.25e1
  variant carriers: 506
genotype quality: GenotypeQuality
  all individuals: 1443
  bin: 3.75e1
  variant carriers: 1079
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 7.25e1
  variant carriers: 425
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 1.25e1
  variant carriers: 224
genotype quality: GenotypeQuality
  all individuals: 1685
  bin: 5.25e1
  variant carriers: 1173
genotype quality: GenotypeQuality
  all individuals: 1374
  bin: 6.75e1
  variant carriers: 837
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 7.5e0
  variant carriers: 202
num of homozygotes: 9622
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP

1-66732389-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732389
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732389
    reference: chr 1
allele count: 5
allele frequency: 6.514827747954345e-5
allele num: 76748
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+619C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.295C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.333C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+619C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+619C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+619C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+619C>G
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13168
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17898
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7104
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12048
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1508
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1243
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2259
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17492
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1910
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2302
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum

1-66732390-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732390
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732390
    reference: chr 1
allele count: 6
allele frequency: 7.848882842342106e-5
allele num: 76444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+620T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.296T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+620T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+620T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.334T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+620T>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+620T>G
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18036
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12931
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2671
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12246
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25093
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2352
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1532
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1245
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1889
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

1-66732394-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732394
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732394
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 74320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.338G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+624G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+624G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+624G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+624G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.300G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+624G>A
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13446
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18830
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1273
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2549
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1754
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1765
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

1-66732398-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732398
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732398
    reference: chr 1
allele count: 1
allele frequency: 1.369562835542895e-5
allele num: 73016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+628G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+628G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+628G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.342G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+628G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.304G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+628G>A
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 2.5e0
  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
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
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genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6268
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 3.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
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genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2675
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1941
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1680
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

1-66732400-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732400
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732400
    reference: chr 1
allele count: 1
allele frequency: 1.382743362831858e-5
allele num: 72320
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+630A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+630A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+630A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.306A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.344A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+630A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+630A>G
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9727
  bin: 2.25e1
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genotype depth: GenotypeDepth
  all individuals: 458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
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genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1466
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 6022
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genotype depth: GenotypeDepth
  all individuals: 187
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 19607
  bin: 7.5e0
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genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
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genotype quality: GenotypeQuality
  all individuals: 299
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genotype quality: GenotypeQuality
  all individuals: 305
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genotype quality: GenotypeQuality
  all individuals: 2064
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genotype quality: GenotypeQuality
  all individuals: 1402
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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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 27913
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

1-66732404-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732404
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732404
    reference: chr 1
allele count: 34
allele frequency: 4.843304843304843e-4
allele num: 70200
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+634G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+634G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+634G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.310G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+634G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.348G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+634G>A
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 265
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 9
genotype depth: GenotypeDepth
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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
  all individuals: 1538
  bin: 6.75e1
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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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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: 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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  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 1427
  bin: 9.75e1
  variant carriers: 29
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

1-66732421-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732421
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732421
    reference: chr 1
allele count: 2
allele frequency: 3.152088258471237e-5
allele num: 63450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+651C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.327C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+651C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+651C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.365C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+651C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+651C>T
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
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genotype depth: GenotypeDepth
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  bin: 7.25e1
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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 quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 291
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1181
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 406
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 4453
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

1-66732423-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732423
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732423
    reference: chr 1
allele count: 1
allele frequency: 1.585137748470342e-5
allele num: 63086
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+653A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.367A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+653A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+653A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+653A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.329A>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+653A>G
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21629
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1167
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30678
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3255
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

1-66732424-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732424
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732424
    reference: chr 1
allele count: 670
allele frequency: 1.073614716533667e-2
allele num: 62406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.368T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+654T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+654T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+654T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.330T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+654T>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+654T>C
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 3.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 2.75e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 2.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 21612
  bin: 7.5e0
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 17346
  bin: 1.25e1
  variant carriers: 147
genotype depth: GenotypeDepth
  all individuals: 101
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 1.75e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 3.75e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 8.25e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 8.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 7306
  bin: 6.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 4.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 30054
  bin: 2.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1113
  bin: 6.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 3243
  bin: 2.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 7.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 2972
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 1.25e1
  variant carriers: 1
num of homozygotes: 21
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

1-66732428-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732428
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732428
    reference: chr 1
allele count: 8
allele frequency: 1.324152542372881e-4
allele num: 60416
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.372G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+658G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+658G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+658G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+658G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.334G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+658G>A
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17280
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 21916
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2372
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5858
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1294
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3035
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 1526
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 30077
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6983
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

1-66732437-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732437
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732437
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 55754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.381G>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+667G>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+667G>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.343G>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+667G>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+667G>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+667G>T
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 22245
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6962
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16698
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1283
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1308
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3357
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7809
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ

1-66732445-ATTC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732445
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732442
    reference: chr 1
allele count: 964
allele frequency: 1.838852433999695e-2
allele num: 52424
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.358_360delTTC
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+682_634+684delTTC
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+682_358+684delTTC
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+682_634+684delTTC
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+682_589+684delTTC
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.396_398delTTC
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+682_634+684delTTC
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 3.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 15512
  bin: 1.25e1
  variant carriers: 552
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 1.75e1
  variant carriers: 166
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 2.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 2.25e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 22774
  bin: 7.5e0
  variant carriers: 540
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8330
  bin: 2.5e0
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 7.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 8.25e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9035
  bin: 7.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3412
  bin: 2.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 1676
  bin: 3.75e1
  variant carriers: 37
genotype quality: GenotypeQuality
  all individuals: 23618
  bin: 2.25e1
  variant carriers: 6
num of homozygotes: 17
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: ATTC
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-66732461-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66732461
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66732461
    reference: chr 1
allele count: 2
allele frequency: 4.450378282153983e-5
allele num: 44940
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000371048
  gene symbol: PDE4B
  hgvsc: ENST00000371048.3:n.405A>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184588
  ensembl transcript: ENST00000490695
  gene symbol: PDE4B
  hgvsc: ENST00000490695.1:n.367A>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.589+691A>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.634+691A>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.634+691A>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.358+691A>C
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.634+691A>C
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8872
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25598
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12493
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3613
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10135
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15151
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2027
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8496
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

1-66798028-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66798028
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66798028
    reference: chr 1
allele count: 1
allele frequency: 8.56956775100264e-6
allele num: 116692
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.635-163T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000431909
  ensembl transcript: ENST00000528771
  gene symbol: PDE4B
  hgvsc: ENST00000528771.1:c.-23-163T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.635-163T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000437249
  ensembl transcript: ENST00000531025
  gene symbol: PDE4B
  hgvsc: ENST00000531025.1:c.-21+86T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.359-163T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.635-163T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.590-163T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360084
  ensembl transcript: ENST00000371045
  gene symbol: PDE4B
  hgvsc: ENST00000371045.5:c.-45T>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000436104
  ensembl transcript: ENST00000526197
  gene symbol: PDE4B
  hgvsc: ENST00000526197.1:c.-24+86T>A
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14756
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1683
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4413
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 901
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

1-66798037-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66798037
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66798037
    reference: chr 1
allele count: 4
allele frequency: 3.418160687733931e-5
allele num: 117022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000437249
  ensembl transcript: ENST00000531025
  gene symbol: PDE4B
  hgvsc: ENST00000531025.1:c.-21+95G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000431909
  ensembl transcript: ENST00000528771
  gene symbol: PDE4B
  hgvsc: ENST00000528771.1:c.-23-154G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360084
  ensembl transcript: ENST00000371045
  gene symbol: PDE4B
  hgvsc: ENST00000371045.5:c.-36G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000436104
  ensembl transcript: ENST00000526197
  gene symbol: PDE4B
  hgvsc: ENST00000526197.1:c.-24+95G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.359-154G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.635-154G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.635-154G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.635-154G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.590-154G>A
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5951
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26597
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1040
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2768
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

1-66798058-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66798058
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66798058
    reference: chr 1
allele count: 1
allele frequency: 8.386166180269028e-6
allele num: 119244
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000436104
  ensembl transcript: ENST00000526197
  gene symbol: PDE4B
  hgvsc: ENST00000526197.1:c.-24+116G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000437249
  ensembl transcript: ENST00000531025
  gene symbol: PDE4B
  hgvsc: ENST00000531025.1:c.-21+116G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.635-133G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360084
  ensembl transcript: ENST00000371045
  gene symbol: PDE4B
  hgvsc: ENST00000371045.5:c.-15G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.635-133G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.359-133G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000431909
  ensembl transcript: ENST00000528771
  gene symbol: PDE4B
  hgvsc: ENST00000528771.1:c.-23-133G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.590-133G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.635-133G>A
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 49356
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

1-66798064-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66798064
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66798064
    reference: chr 1
allele count: 724
allele frequency: 6.036552828175027e-3
allele num: 119936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000437249
  ensembl transcript: ENST00000531025
  gene symbol: PDE4B
  hgvsc: ENST00000531025.1:c.-21+122G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000431909
  ensembl transcript: ENST00000528771
  gene symbol: PDE4B
  hgvsc: ENST00000528771.1:c.-23-127G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.635-127G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.635-127G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.359-127G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000436104
  ensembl transcript: ENST00000526197
  gene symbol: PDE4B
  hgvsc: ENST00000526197.1:c.-24+122G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.635-127G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360084
  ensembl transcript: ENST00000371045
  gene symbol: PDE4B
  hgvsc: ENST00000371045.5:c.-9G>A
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.590-127G>A
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20158
  bin: 2.75e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 32700
  bin: 2.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 5.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.25e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 4311
  bin: 3.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.75e1
  variant carriers: 115
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 12
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

1-66798082-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66798082
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66798082
    reference: chr 1
allele count: 8
allele frequency: 6.640988179041042e-5
allele num: 120464
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360084
  ensembl transcript: ENST00000371045
  gene symbol: PDE4B
  hgvsc: ENST00000371045.5:c.10C>G
  hgvsp: ENSP00000360084.5:p.His4Asp
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000436104
  ensembl transcript: ENST00000526197
  gene symbol: PDE4B
  hgvsc: ENST00000526197.1:c.-23-109C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.635-109C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.635-109C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000431909
  ensembl transcript: ENST00000528771
  gene symbol: PDE4B
  hgvsc: ENST00000528771.1:c.-23-109C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.359-109C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000437249
  ensembl transcript: ENST00000531025
  gene symbol: PDE4B
  hgvsc: ENST00000531025.1:c.-20-112C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.635-109C>G
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.590-109C>G
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 20864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His4Asp
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

1-66798084-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66798084
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66798084
    reference: chr 1
allele count: 3
allele frequency: 2.489957172736629e-5
allele num: 120484
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.635-107C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.635-107C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360084
  ensembl transcript: ENST00000371045
  gene symbol: PDE4B
  hgvsc: ENST00000371045.5:c.12C>T
  hgvsp: ENST00000371045.5:c.12C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000437249
  ensembl transcript: ENST00000531025
  gene symbol: PDE4B
  hgvsc: ENST00000531025.1:c.-20-110C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.635-107C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.590-107C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000431909
  ensembl transcript: ENST00000528771
  gene symbol: PDE4B
  hgvsc: ENST00000528771.1:c.-23-107C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000436104
  ensembl transcript: ENST00000526197
  gene symbol: PDE4B
  hgvsc: ENST00000526197.1:c.-23-107C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.359-107C>T
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 8.25e1
  variant carriers: 0
hgvs: p.His4His
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

1-66798097-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66798097
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66798097
    reference: chr 1
allele count: 1
allele frequency: 8.288025460814215e-6
allele num: 120656
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.635-94A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.590-94A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360084
  ensembl transcript: ENST00000371045
  gene symbol: PDE4B
  hgvsc: ENST00000371045.5:c.25A>T
  hgvsp: ENSP00000360084.5:p.Ser9Cys
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.635-94A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.359-94A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000437249
  ensembl transcript: ENST00000531025
  gene symbol: PDE4B
  hgvsc: ENST00000531025.1:c.-20-97A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000431909
  ensembl transcript: ENST00000528771
  gene symbol: PDE4B
  hgvsc: ENST00000528771.1:c.-23-94A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.635-94A>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000436104
  ensembl transcript: ENST00000526197
  gene symbol: PDE4B
  hgvsc: ENST00000526197.1:c.-23-94A>T
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5189
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser9Cys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ

1-66798105-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66798105
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 66798105
    reference: chr 1
allele count: 4
allele frequency: 3.313727114572115e-5
allele num: 120710
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000431909
  ensembl transcript: ENST00000528771
  gene symbol: PDE4B
  hgvsc: ENST00000528771.1:c.-23-86C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360084
  ensembl transcript: ENST00000371045
  gene symbol: PDE4B
  hgvsc: ENST00000371045.5:c.33C>T
  hgvsp: ENST00000371045.5:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000392947
  ensembl transcript: ENST00000423207
  gene symbol: PDE4B
  hgvsc: ENST00000423207.2:c.590-86C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000397548
  ensembl transcript: ENST00000412480
  gene symbol: PDE4B
  hgvsc: ENST00000412480.2:c.359-86C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000332116
  ensembl transcript: ENST00000329654
  gene symbol: PDE4B
  hgvsc: ENST00000329654.4:c.635-86C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000436104
  ensembl transcript: ENST00000526197
  gene symbol: PDE4B
  hgvsc: ENST00000526197.1:c.-23-86C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000360088
  ensembl transcript: ENST00000371049
  gene symbol: PDE4B
  hgvsc: ENST00000371049.3:c.635-86C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000342637
  ensembl transcript: ENST00000341517
  gene symbol: PDE4B
  hgvsc: ENST00000341517.4:c.635-86C>T
  variant of: http://identifiers.org/hgnc/8781
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184588
  ensembl protein: ENSP00000437249
  ensembl transcript: ENST00000531025
  gene symbol: PDE4B
  hgvsc: ENST00000531025.1:c.-20-89C>T
  variant of: http://identifiers.org/hgnc/8781
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32899
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr11Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C

GenotypeQuality
all individuals: 482
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4185
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5893
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24209
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2071
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 892
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11246
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532379171902295e-5
allele num: 65258
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16308
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.03e-1

QD
type: SiteQuality
SIO_000300: 1.472e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.564e0

DP
type: SiteQuality
SIO_000300: 1.782014e6

GenotypeQuality
all individuals: 5831
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1704
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1708
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3553
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4325
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15583
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4973
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5891
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1002
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10106
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16270
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11168
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.543686322939179e-5
allele num: 64780
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.258e0

QD
type: SiteQuality
SIO_000300: 8.869999999999999e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.639e0

MQRankSum
type: SiteQuality
SIO_000300: -1.331e0

DP
type: SiteQuality
SIO_000300: 1.680035e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.359e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e0

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 816
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6200
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35215
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1638
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2028
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2302
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3995
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.014772384684956e-5
allele num: 66340
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQRankSum
type: SiteQuality
SIO_000300: 2.1e0

VQSLOD
type: SiteQuality
SIO_000300: -7.935e-1

DP
type: SiteQuality
SIO_000300: 1.696915e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.01e-1

QD
type: SiteQuality
SIO_000300: 1.413e1

GenotypeQuality
all individuals: 332
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6077
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40811
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1627
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1443
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.218026796589525e-4
allele num: 16420
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66426
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.69e-1

QD
type: SiteQuality
SIO_000300: 1.097e1

ClippingRankSum
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SIO_000300: 1.12e0

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.92e0

DP
type: SiteQuality
SIO_000300: 1.709457e6

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.164144353899884e-4
allele num: 8590
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66430
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.29e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

FS
type: SiteQuality
SIO_000300: 1.992e0

VQSLOD
type: SiteQuality
SIO_000300: 6.43e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.118e0

DP
type: SiteQuality
SIO_000300: 1.710913e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66442
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.596e0

MQ
type: SiteQuality
SIO_000300: 5.339e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.452e0

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -3.09e-1

QD
type: SiteQuality
SIO_000300: 2.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.599999999999999e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 33

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: 10330
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504800312998465e-5
allele num: 66454
num of homozygotes: 0

South Asian
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allele count: 33
allele frequency: 2.009010105929624e-3
allele num: 16426
num of homozygotes: 1

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.724082e6

QD
type: SiteQuality
SIO_000300: 1.434e1

VQSLOD
type: SiteQuality
SIO_000300: 4.43e0

MQRankSum
type: SiteQuality
SIO_000300: -1.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.09e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.11e-1

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504392827055001e-5
allele num: 66472
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.937e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e-1

DP
type: SiteQuality
SIO_000300: 1.728098e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.67e-1

QD
type: SiteQuality
SIO_000300: 6.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 1.0772e1

MQRankSum
type: SiteQuality
SIO_000300: 1.93e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.491e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.654373431164318e-5
allele num: 10358
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66506
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.508e1

DP
type: SiteQuality
SIO_000300: 1.734471e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.14e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.291e0

VQSLOD
type: SiteQuality
SIO_000300: -5.502e-1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503623733197005e-5
allele num: 66506
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.736887e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

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

European (Finnish)
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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
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503126503126503e-5
allele num: 66528
num of homozygotes: 0

East Asian
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allele count: 0
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MQRankSum
type: SiteQuality
SIO_000300: -7.0e-1

FS
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.23e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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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

Latino
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East Asian
type: Population
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Other
type: Population
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.503081316699233e-5
allele num: 66530
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South Asian
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BaseQRankSum
type: SiteQuality
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MQ
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ReadPosRankSum
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QD
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FS
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InbreedingCoeff
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DP
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ClippingRankSum
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MQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6560
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African
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allele frequency: 0.0e0
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Latino
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Other
type: Population
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South Asian
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allele frequency: 6.075334143377886e-5
allele num: 16460
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66548
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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DP
type: SiteQuality
SIO_000300: 1.740845e6

FS
type: SiteQuality
SIO_000300: 1.421e0

VQSLOD
type: SiteQuality
SIO_000300: 3.24e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.91e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.01e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.104e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.59e-1

QD
type: SiteQuality
SIO_000300: 8.1e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.682062858135092e-5
allele num: 11518
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66562
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.788e0

DP
type: SiteQuality
SIO_000300: 1.742576e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.01e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.623e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.15e-1

QD
type: SiteQuality
SIO_000300: 1.144e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.193e0

VQSLOD
type: SiteQuality
SIO_000300: 8.91e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004717406327935e-5
allele num: 66562
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: -2.35e-1

FS
type: SiteQuality
SIO_000300: 1.094e0

QD
type: SiteQuality
SIO_000300: 1.333e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.57e-1

DP
type: SiteQuality
SIO_000300: 1.74265e6

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 8.89e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.744717e6

QD
type: SiteQuality
SIO_000300: 9.609999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.718e0

VQSLOD
type: SiteQuality
SIO_000300: -5.32e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.141e0

MQRankSum
type: SiteQuality
SIO_000300: 6.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.53e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.072382803011902e-5
allele num: 16468
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66594
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.652e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.328e0

DP
type: SiteQuality
SIO_000300: 1.744757e6

MQRankSum
type: SiteQuality
SIO_000300: 2.99e0

FS
type: SiteQuality
SIO_000300: 6.234e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.105e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.161710037174721e-4
allele num: 8608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 6.19e-1

DP
type: SiteQuality
SIO_000300: 1.745027e6

FS
type: SiteQuality
SIO_000300: 6.913e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.347e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.437e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.129e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501501501501501e-5
allele num: 66600
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 7.75e0

FS
type: SiteQuality
SIO_000300: 1.893e0

DP
type: SiteQuality
SIO_000300: 1.745171e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.759e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.12e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.14e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.521606816798539e-4
allele num: 6572
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66570
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.942e1

MQRankSum
type: SiteQuality
SIO_000300: -5.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.16e-1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.06e-1

QD
type: SiteQuality
SIO_000300: 1.055e1

FS
type: SiteQuality
SIO_000300: 5.427e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.8e0

DP
type: SiteQuality
SIO_000300: 1.745164e6

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.091617933723197e-5
allele num: 16416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66484
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.126e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.599999999999999e-3

FS
type: SiteQuality
SIO_000300: 5.325e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.18e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.851e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 7.88e0

DP
type: SiteQuality
SIO_000300: 1.742834e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 50
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GenotypeQuality
all individuals: 44751
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.105751618024179e-5
allele num: 16378
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66398
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

FS
type: SiteQuality
SIO_000300: 7.405e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-1

MQ
type: SiteQuality
SIO_000300: 5.926e1

QD
type: SiteQuality
SIO_000300: 1.064e1

VQSLOD
type: SiteQuality
SIO_000300: -7.72e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

DP
type: SiteQuality
SIO_000300: 1.740887e6

GenotypeQuality
all individuals: 76
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 736
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 27
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GenotypeQuality
all individuals: 1314
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507704369327262e-5
allele num: 66326
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.738172e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

MQ
type: SiteQuality
SIO_000300: 5.944e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.88e-1

FS
type: SiteQuality
SIO_000300: 9.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.305e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.337e0

VQSLOD
type: SiteQuality
SIO_000300: 4.17e-1

QD
type: SiteQuality
SIO_000300: 1.373e1

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.759906304899473e-5
allele num: 10246
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66198
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

FS
type: SiteQuality
SIO_000300: 8.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.37e0

VQSLOD
type: SiteQuality
SIO_000300: -4.152e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.44e0

MQ
type: SiteQuality
SIO_000300: 5.92e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e0

DP
type: SiteQuality
SIO_000300: 1.734259e6

QD
type: SiteQuality
SIO_000300: 1.125e1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 443
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.602718210084303e-5
allele num: 62394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15432
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8048
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6252
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.407337723424271e-5
allele num: 10630
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 1.591333e6

FS
type: SiteQuality
SIO_000300: 3.252e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

VQSLOD
type: SiteQuality
SIO_000300: 6.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.51e0

QD
type: SiteQuality
SIO_000300: 1.423e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 5

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

GenotypeQuality
all individuals: 473
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variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.26594598125347e-5
allele num: 61238
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7850
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6192
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.170577045022194e-4
allele num: 9462
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.73e-1

QD
type: SiteQuality
SIO_000300: 1.404e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

FS
type: SiteQuality
SIO_000300: 5.763e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.538121e6

GenotypeQuality
all individuals: 3809
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 325
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15060
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6106
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9336
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10170
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7680
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.661350345560872e-5
allele num: 60192
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.19e0

QD
type: SiteQuality
SIO_000300: 2.024e1

MQRankSum
type: SiteQuality
SIO_000300: 1.95e-1

DP
type: SiteQuality
SIO_000300: 1.486718e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.419999999999999e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14742
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.4296788482835e-4
allele num: 9030
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5962
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7266
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57902
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.17e-1

FS
type: SiteQuality
SIO_000300: 3.152e0

MQRankSum
type: SiteQuality
SIO_000300: 2.92e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.346049e6

VQSLOD
type: SiteQuality
SIO_000300: 7.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

QD
type: SiteQuality
SIO_000300: 1.402e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.13e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14666
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5940
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8978
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.689305203155956e-5
allele num: 57542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.33e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.324717e6

MQRankSum
type: SiteQuality
SIO_000300: 2.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

FS
type: SiteQuality
SIO_000300: 3.022e0

QD
type: SiteQuality
SIO_000300: 1.277e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.81e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.496e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5916
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 2.09643605870021e-4
allele num: 9540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57248
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8910
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.303609e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.89e-1

FS
type: SiteQuality
SIO_000300: 2.171e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 32

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 704
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GenotypeQuality
all individuals: 4772
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 682
num of homozygotes: 0

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

South Asian
type: Population
allele count: 32
allele frequency: 2.45474071801166e-3
allele num: 13036
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7810
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5654
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

DP
type: SiteQuality
SIO_000300: 1.048118e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.77e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.800000000000001e-3

QD
type: SiteQuality
SIO_000300: 1.404e1

GenotypeQuality
all individuals: 2107
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27928
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3972
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.047559187094071e-4
allele num: 9546
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3918
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.35e-2

QD
type: SiteQuality
SIO_000300: 4.72e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.936e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.5691e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.51e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 100
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variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27980
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4124
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3996
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4182
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.092487968194183e-4
allele num: 9558
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3920
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.29e0

DP
type: SiteQuality
SIO_000300: 6.68752e5

MQRankSum
type: SiteQuality
SIO_000300: -1.137e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.41e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.16e-1

MQ
type: SiteQuality
SIO_000300: 5.515e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.46e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 1

GenotypeQuality
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bin: 9.75e1
variant carriers: 15

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: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 103
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variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28676
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3988
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4250
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 1.435014350143502e-3
allele num: 9756
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 480
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.313e1

VQSLOD
type: SiteQuality
SIO_000300: 6.909999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

FS
type: SiteQuality
SIO_000300: 3.285e0

DP
type: SiteQuality
SIO_000300: 6.80661e5

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.37e-1

GenotypeQuality
all individuals: 259
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 107
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GenotypeQuality
all individuals: 1264
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3998
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4300
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4244
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9702
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4134
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 476
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.18e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.48e-1

DP
type: SiteQuality
SIO_000300: 6.90857e5

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.863e1

GenotypeQuality
all individuals: 5420
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 923
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2494
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variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.643635397289396e-5
allele num: 30104
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4390
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4104
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10006
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.72e-1

DP
type: SiteQuality
SIO_000300: 7.5368e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.55e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.46e-1

QD
type: SiteQuality
SIO_000300: 1.382e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.76e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

GenotypeQuality
all individuals: 228
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2824
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1094
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4424
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.990313806143435e-4
allele num: 30146
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4104
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4354
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.879e0

VQSLOD
type: SiteQuality
SIO_000300: -1.651e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.017e0

MQRankSum
type: SiteQuality
SIO_000300: 3.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.02e-1

DP
type: SiteQuality
SIO_000300: 7.62093e5

FS
type: SiteQuality
SIO_000300: 1.2052e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-3

QD
type: SiteQuality
SIO_000300: 5.78e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10986
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.314233144959916e-4
allele num: 30436
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4640
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4404
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.423e0

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.269e0

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.373e0

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.95e1

DP
type: SiteQuality
SIO_000300: 7.70588e5

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4796
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4366
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 32904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4796
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.666e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

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

VQSLOD
type: SiteQuality
SIO_000300: 2.66e-1

FS
type: SiteQuality
SIO_000300: 5.0e0

DP
type: SiteQuality
SIO_000300: 8.37113e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.62e-1

GenotypeQuality
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variant carriers: 1

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 5306
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10636
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4406
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4922
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 1
allele frequency: 2.028397565922921e-4
allele num: 4930
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33846
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.222e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.165e0

VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.035e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.71e-1

DP
type: SiteQuality
SIO_000300: 8.55876e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1466
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GenotypeQuality
all individuals: 131
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10766
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.743825387708214e-5
allele num: 34820
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5022
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5028
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5484
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 530
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.89e-1

QD
type: SiteQuality
SIO_000300: 1.111e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -6.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.97e-1

MQ
type: SiteQuality
SIO_000300: 5.829e1

DP
type: SiteQuality
SIO_000300: 8.71711e5

FS
type: SiteQuality
SIO_000300: 1.48e0

VQSLOD
type: SiteQuality
SIO_000300: 2.7e0

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

GenotypeQuality
all individuals: 477
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3105
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1226
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 3.977724741447892e-4
allele num: 5028
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5022
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10766
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34820
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5484
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

DP
type: SiteQuality
SIO_000300: 8.71711e5

BaseQRankSum
type: SiteQuality
SIO_000300: -6.97e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.97e-1

FS
type: SiteQuality
SIO_000300: 1.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.89e-1

QD
type: SiteQuality
SIO_000300: 1.111e1

VQSLOD
type: SiteQuality
SIO_000300: 2.7e0

MQ
type: SiteQuality
SIO_000300: 5.829e1

GenotypeQuality
all individuals: 169
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 584
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1673
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19707
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1140
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5932
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.727471088806459e-5
allele num: 36664
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11062
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4688
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5228
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 550
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.27e0

MQRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

FS
type: SiteQuality
SIO_000300: 2.046e0

DP
type: SiteQuality
SIO_000300: 9.08452e5

QD
type: SiteQuality
SIO_000300: 6.23e0

GenotypeQuality
all individuals: 2478
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21329
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22045
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5388
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.824151769427216e-4
allele num: 5482
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11308
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4838
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38304
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.796e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e0

QD
type: SiteQuality
SIO_000300: 1.623e1

VQSLOD
type: SiteQuality
SIO_000300: 7.199999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.928e1

DP
type: SiteQuality
SIO_000300: 9.31934e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.47e-1

GenotypeQuality
all individuals: 21468
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1186
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2450
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1230
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 635
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1763
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6280
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5416
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4852
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.596728122565568e-5
allele num: 38510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.58e-1

MQ
type: SiteQuality
SIO_000300: 5.915e1

QD
type: SiteQuality
SIO_000300: 9.57e0

FS
type: SiteQuality
SIO_000300: 1.971e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.952e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

MQRankSum
type: SiteQuality
SIO_000300: -1.655e0

DP
type: SiteQuality
SIO_000300: 9.36081e5

GenotypeQuality
all individuals: 1784
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1234
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1190
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2444
bin: 3.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4892
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5442
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6382
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 7.674204440806303e-5
allele num: 39092
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.799718409010911e-5
allele num: 11364
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.99e0

DP
type: SiteQuality
SIO_000300: 9.44295e5

MQRankSum
type: SiteQuality
SIO_000300: -3.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.589e0

QD
type: SiteQuality
SIO_000300: 8.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.166e0

GenotypeQuality
all individuals: 516
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1359
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1324
bin: 9.75e1
variant carriers: 93

GenotypeQuality
all individuals: 21411
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 152
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 175
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 514
bin: 5.75e1
variant carriers: 1

Other
type: Population
allele count: 1
allele frequency: 1.730103806228374e-3
allele num: 578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.505637684790779e-5
allele num: 39910
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5698
num of homozygotes: 0

African
type: Population
allele count: 97
allele frequency: 1.740222461428059e-2
allele num: 5574
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 6.11807892321811e-4
allele num: 6538
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.713837574067619e-5
allele num: 11476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4956
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.5511e5

QD
type: SiteQuality
SIO_000300: 1.011e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.056e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e-1

FS
type: SiteQuality
SIO_000300: 5.45e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

MQ
type: SiteQuality
SIO_000300: 5.805e1

GenotypeQuality
all individuals: 601
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1134
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1466
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 873
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1863
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21025
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5566
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4984
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5752
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.682062858135092e-5
allele num: 11518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40318
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.684e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.064e0

MQRankSum
type: SiteQuality
SIO_000300: 7.45e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.371e1

FS
type: SiteQuality
SIO_000300: 2.039e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.7e-1

DP
type: SiteQuality
SIO_000300: 9.57678e5

GenotypeQuality
all individuals: 570
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1507
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1142
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1869
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.949025042066713e-5
allele num: 40412
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4990
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5758
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.59516e5

MQ
type: SiteQuality
SIO_000300: 5.878e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

QD
type: SiteQuality
SIO_000300: 9.550000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

FS
type: SiteQuality
SIO_000300: 9.093e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.197e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.02e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.49e0

GenotypeQuality
all individuals: 770
bin: 4.25e1
variant carriers: 602

GenotypeQuality
all individuals: 1416
bin: 4.75e1
variant carriers: 1133

GenotypeQuality
all individuals: 532
bin: 8.75e1
variant carriers: 499

GenotypeQuality
all individuals: 1196
bin: 2.5e0
variant carriers: 138

GenotypeQuality
all individuals: 851
bin: 7.75e1
variant carriers: 682

GenotypeQuality
all individuals: 1139
bin: 2.75e1
variant carriers: 399

GenotypeQuality
all individuals: 23883
bin: 9.75e1
variant carriers: 23648

GenotypeQuality
all individuals: 1480
bin: 3.25e1
variant carriers: 816

GenotypeQuality
all individuals: 639
bin: 9.25e1
variant carriers: 606

GenotypeQuality
all individuals: 8147
bin: 6.25e1
variant carriers: 1093

East Asian
type: Population
allele count: 1219
allele frequency: 1.975688816855754e-1
allele num: 6170
num of homozygotes: 90

European (Non-Finnish)
type: Population
allele count: 29223
allele frequency: 5.546634779637855e-1
allele num: 52686
num of homozygotes: 7385

African
type: Population
allele count: 1402
allele frequency: 2.306679828891083e-1
allele num: 6078
num of homozygotes: 126

Latino
type: Population
allele count: 2462
allele frequency: 3.130722278738555e-1
allele num: 7864
num of homozygotes: 290

European (Finnish)
type: Population
allele count: 3381
allele frequency: 5.728566587597425e-1
allele num: 5902
num of homozygotes: 918

Other
type: Population
allele count: 313
allele frequency: 4.589442815249267e-1
allele num: 682
num of homozygotes: 70

South Asian
type: Population
allele count: 4465
allele frequency: 3.447876447876448e-1
allele num: 12950
num of homozygotes: 743

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.06e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.73e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-2

QD
type: SiteQuality
SIO_000300: 1.814e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.258829e6

GenotypeQuality
all individuals: 365
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24820
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1411
bin: 9.75e1
variant carriers: 6

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.203948952564411e-4
allele num: 41530
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4998
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11690
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5522
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5790
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.69248e5

QD
type: SiteQuality
SIO_000300: 1.56e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.62e-1

FS
type: SiteQuality
SIO_000300: 3.751e0

MQ
type: SiteQuality
SIO_000300: 5.805e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.8e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.553e0

MQRankSum
type: SiteQuality
SIO_000300: -5.31e-1

GenotypeQuality
all individuals: 560
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2294
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17275
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1411
bin: 9.75e1
variant carriers: 6

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5766
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11670
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.451449029948232e-4
allele num: 41338
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4984
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.25e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.828e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

DP
type: SiteQuality
SIO_000300: 9.64084e5

FS
type: SiteQuality
SIO_000300: 2.388e0

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.031e0

MQ
type: SiteQuality
SIO_000300: 5.805e1

QD
type: SiteQuality
SIO_000300: 2.97e1

GenotypeQuality
all individuals: 139
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1403
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14879
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26469
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 592
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2514
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5344
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.33028e5

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.642e1

VQSLOD
type: SiteQuality
SIO_000300: -7.956e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQ
type: SiteQuality
SIO_000300: 5.303e1

GenotypeQuality
all individuals: 463
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14218
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2591
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1405
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39264
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5264
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4814
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.624431448992852e-4
allele num: 6156
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.011e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.558e0

VQSLOD
type: SiteQuality
SIO_000300: 8.0e-4

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.51e-1

DP
type: SiteQuality
SIO_000300: 9.15287e5

MQ
type: SiteQuality
SIO_000300: 5.889e1

MQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.25e-1

GenotypeQuality
all individuals: 810
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2645
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2763
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38870
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6046
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5216
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.821453775582216e-5
allele num: 11336
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4786
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.609e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -9.721e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.02317e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

FS
type: SiteQuality
SIO_000300: 2.43e0

QD
type: SiteQuality
SIO_000300: 9.5e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 2879
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 326
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2716
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1230
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28686
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4686
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5826
num of homozygotes: 0

East Asian
type: Population
allele count: 32
allele frequency: 5.983545250560957e-3
allele num: 5348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5054
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.792757260666906e-4
allele num: 11156
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.664e0

QD
type: SiteQuality
SIO_000300: 8.699999999999999e0

DP
type: SiteQuality
SIO_000300: 8.76886e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.485e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.54e-1

MQ
type: SiteQuality
SIO_000300: 5.896e1

MQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

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

GenotypeQuality
all individuals: 1028
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7996
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1397
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1365
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2929
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4806
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4706
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33434
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.88465887674331e-4
allele num: 10612
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5006
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 526
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.119e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.800000000000001e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.67e-1

QD
type: SiteQuality
SIO_000300: 2.576e1

MQ
type: SiteQuality
SIO_000300: 5.395e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.913e0

DP
type: SiteQuality
SIO_000300: 7.91821e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e-1

GenotypeQuality
all individuals: 225
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7874
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4686
bin: 7.5e0
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GenotypeQuality
all individuals: 360
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GenotypeQuality
all individuals: 1396
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variant carriers: 1

GenotypeQuality
all individuals: 1100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
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variant carriers: 0

GenotypeQuality
all individuals: 1325
bin: 1.75e1
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GenotypeQuality
all individuals: 2951
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4354
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33226
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4780
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4700
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.455370650529501e-5
allele num: 10576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4926
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.25e-1

MQ
type: SiteQuality
SIO_000300: 5.823e1

QD
type: SiteQuality
SIO_000300: 1.696e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.06e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.483e0

MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

FS
type: SiteQuality
SIO_000300: 1.085e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.97e-1

DP
type: SiteQuality
SIO_000300: 7.84856e5

GenotypeQuality
all individuals: 5047
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 1112
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 224
bin: 5.25e1
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GenotypeQuality
all individuals: 1530
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 403
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 9.25e1
variant carriers: 28

GenotypeQuality
all individuals: 235
bin: 4.75e1
variant carriers: 5

GenotypeQuality
all individuals: 351
bin: 7.25e1
variant carriers: 13

GenotypeQuality
all individuals: 1897
bin: 9.75e1
variant carriers: 609

GenotypeQuality
all individuals: 210
bin: 5.75e1
variant carriers: 3

Other
type: Population
allele count: 3
allele frequency: 5.791505791505791e-3
allele num: 518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.525413387027885e-4
allele num: 32778
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4724
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 1.029654036243822e-3
allele num: 4856
num of homozygotes: 0

South Asian
type: Population
allele count: 656
allele frequency: 6.218009478672986e-2
allele num: 10550
num of homozygotes: 21

African
type: Population
allele count: 1
allele frequency: 2.152389151958674e-4
allele num: 4646
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.186e0

QD
type: SiteQuality
SIO_000300: 1.106e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.27e0

MQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

FS
type: SiteQuality
SIO_000300: 1.422e0

DP
type: SiteQuality
SIO_000300: 7.767e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e-1

GenotypeQuality
all individuals: 1111
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 5.25e1
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GenotypeQuality
all individuals: 350
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GenotypeQuality
all individuals: 1399
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GenotypeQuality
all individuals: 368
bin: 2.5e0
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GenotypeQuality
all individuals: 222
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GenotypeQuality
all individuals: 132
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GenotypeQuality
all individuals: 1095
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GenotypeQuality
all individuals: 114
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GenotypeQuality
all individuals: 208
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10164
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.131287297527707e-4
allele num: 4692
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 1.537785588752197e-3
allele num: 4552
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31626
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.28e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.67e-1

DP
type: SiteQuality
SIO_000300: 7.54846e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.48e-1

GenotypeQuality
all individuals: 27839
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 239
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2166
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4252
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4238
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28714
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4098
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.69e-2

DP
type: SiteQuality
SIO_000300: 7.14823e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.55e-1

QD
type: SiteQuality
SIO_000300: 5.2e0

FS
type: SiteQuality
SIO_000300: 3.424e0

VQSLOD
type: SiteQuality
SIO_000300: -1.704e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 3284
bin: 1.25e1
variant carriers: 8

GenotypeQuality
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bin: 1.75e1
variant carriers: 11

GenotypeQuality
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bin: 6.25e1
variant carriers: 4

GenotypeQuality
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bin: 7.75e1
variant carriers: 24

GenotypeQuality
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bin: 6.75e1
variant carriers: 7

GenotypeQuality
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bin: 8.75e1
variant carriers: 36

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 8

GenotypeQuality
all individuals: 3396
bin: 3.25e1
variant carriers: 22

GenotypeQuality
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bin: 9.75e1
variant carriers: 1281

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3984
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 716
allele frequency: 2.683457012217975e-2
allele num: 26682
num of homozygotes: 11

Other
type: Population
allele count: 9
allele frequency: 1.991150442477876e-2
allele num: 452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 39
allele frequency: 9.923664122137405e-3
allele num: 3930
num of homozygotes: 1

African
type: Population
allele count: 67
allele frequency: 1.642962236390387e-2
allele num: 4078
num of homozygotes: 2

Latino
type: Population
allele count: 78
allele frequency: 2.124183006535948e-2
allele num: 3672
num of homozygotes: 1

South Asian
type: Population
allele count: 55
allele frequency: 5.713692083939331e-3
allele num: 9626
num of homozygotes: 2

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.54e0

MQ
type: SiteQuality
SIO_000300: 5.668e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

QD
type: SiteQuality
SIO_000300: 1.957e1

MQRankSum
type: SiteQuality
SIO_000300: -5.49e-1

DP
type: SiteQuality
SIO_000300: 6.76188e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-2

GenotypeQuality
all individuals: 3367
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6118
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 251
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variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 5.770340450086555e-4
allele num: 3466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9072
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2770
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22330
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3350
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: -2.032e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.46e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-1

QD
type: SiteQuality
SIO_000300: 2.058e1

FS
type: SiteQuality
SIO_000300: 2.922e0

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

DP
type: SiteQuality
SIO_000300: 6.38277e5

GenotypeQuality
all individuals: 4008
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 2745
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9980
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8254
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11256
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15378
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.550339524355834e-5
allele num: 64502
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.401e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.76e-1

QD
type: SiteQuality
SIO_000300: 1.187e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.28e-1

DP
type: SiteQuality
SIO_000300: 1.317604e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2425
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4512
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 147
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1075
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
all individuals: 2683
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GenotypeQuality
all individuals: 194
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variant carriers: 0

GenotypeQuality
all individuals: 1483
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8280
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.542257865515114e-4
allele num: 6484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.636928498562552e-5
allele num: 64698
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9988
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11266
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.903e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.327e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.376901e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.57e-1

QD
type: SiteQuality
SIO_000300: 1.102e1

GenotypeQuality
all individuals: 342
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 196
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 48
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GenotypeQuality
all individuals: 814
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10138
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522997258604934e-5
allele num: 65660
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16074
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.74e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.355e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.448e0

QD
type: SiteQuality
SIO_000300: 1.757e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

VQSLOD
type: SiteQuality
SIO_000300: -1.294e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

DP
type: SiteQuality
SIO_000300: 1.481094e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 702

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 187
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GenotypeQuality
all individuals: 216
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 6.787330316742082e-3
allele num: 884
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.915454187966968e-4
allele num: 10172
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 146
allele frequency: 2.214268381460811e-3
allele num: 65936
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.864383082838169e-4
allele num: 11444
num of homozygotes: 0

South Asian
type: Population
allele count: 558
allele frequency: 3.41409691629956e-2
allele num: 16344
num of homozygotes: 12

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.32e0

DP
type: SiteQuality
SIO_000300: 1.507349e6

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.2e-2

QD
type: SiteQuality
SIO_000300: 1.419e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.27e-2

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.208422706262651e-4
allele num: 66202
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.975e1

QD
type: SiteQuality
SIO_000300: 1.594e1

FS
type: SiteQuality
SIO_000300: 2.411e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.516e0

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

DP
type: SiteQuality
SIO_000300: 1.507974e6

GenotypeQuality
all individuals: 5159
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 35
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GenotypeQuality
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GenotypeQuality
all individuals: 29
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 33
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GenotypeQuality
all individuals: 895
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.703220191470844e-5
allele num: 11490
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.020509257860875e-5
allele num: 66214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 7.4e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.23e-1

QD
type: SiteQuality
SIO_000300: 1.36e1

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.584e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.69e-1

DP
type: SiteQuality
SIO_000300: 1.508666e6

GenotypeQuality
all individuals: 1055
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 51335
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 901
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507977199384745e-5
allele num: 66314
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.510715e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.81e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.4e-2

QD
type: SiteQuality
SIO_000300: 1.241e1

MQ
type: SiteQuality
SIO_000300: 5.901e1

GenotypeQuality
all individuals: 1059
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 51320
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 900
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5187
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 790
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66346
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.925687536571094e-4
allele num: 10254
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

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

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